Pseudocyesis
Pseudopregnancy
17-Valerate, Betamethasone
5 Formyltetrahydrofolate
Agents, Ganglionic Blocking
Agents, Ganglioplegic
Ageusia
Agitation, Psychomotor
Angle Class II
Anxiety, Separation
Arthritis, Juvenile Chronic
Autoimmune Thrombocytopenic Purpura
Autoimmune Thrombocytopenic Purpuras
Babinski Reflex
Babinski Reflexes
Behavior, Self-Destructive
Betamethasone 17 Valerate
Blockaders, Ganglionic
Blocking Agents, Ganglionic
Bone Tuberculoses
Catarrh, Malignant
Catarrhs, Malignant
Cerebral Hemorrhage
Cerebral Hemorrhages
Chronic Arthritis, Juvenile
Class II, Angle
Cross Transfusion, Intrauterine
Cross-Transfusion, Intrauterine
Cross-Transfusions, Intrauterine
Cystinosis
Cytophosphan
De Toni Debre Fanconi Syndrome
De Toni-Debre-Fanconi Syndrome
Deafness
Deficiencies, Glucosephosphate Dehydrogenase
Deficiencies, GPD
Deficiency, Glucosephosphate Dehydrogenase
Deficiency, GPD
Degeneration, Macular
Degenerations, Macular
Dehydrogenase Deficiencies, Glucosephosphate
Dehydrogenase Deficiency, Glucosephosphate
Di Te Per Vaccine
Di-Te-Per Vaccine
Dihydronorguaiaretic Acid
Diphenylhydantoinate, Sodium
Diphtheria Pertussis Tetanus Vaccine
Diphtheria Tetanus Pertussis Vaccine
Diphtheria-Pertussis-Tetanus Vaccine
Diphtheria-Tetanus-Pertussis Vaccine
Disease, Werlhof
DPT Vaccine
DTP Vaccine
Enteritis, Regional
Excitement, Psychomotor
Fetofetal Transfusion
Fetofetal Transfusions
Flubenisolonvalerate
Galactorrhea
Galactorrheas
Ganglionic Blockaders
Ganglionic Blocking Agents
Ganglioplegic Agents
Glucosephosphate Dehydrogenase Deficiencies
Glucosephosphate Dehydrogenase Deficiency
Goldenhar Syndrome
GPD Deficiencies
GPD Deficiency
Guerin Stern Syndrome
Guerin-Stern Syndrome
Guillain-Barre Syndrome
Hemolytic Disease of Newborn
Hemorrhage, Cerebral
Hemorrhages, Cerebral
Hernia, Hiatal
Hernias, Hiatal
Hiatal Hernia
Hiatal Hernias
Hyper IgE Syndrome
Hyper-IgE Syndrome
Hyper-IgE Syndromes
Hyperimmunoglobulin E-Recurrent Infection Syndrome
Hyperplasia, Prostatic
Hypoventilation
Hypoventilations
Idiopathic Thrombocytopenic Purpura
Idiopathic Thrombocytopenic Purpuras
Infection
Infections
Intrauterine Cross Transfusion
Intrauterine Cross-Transfusion
Intrauterine Cross-Transfusions
Jobs Syndrome
Macular Degeneration
Macular Degenerations
Malignant Catarrh
Malignant Catarrhs
Malocclusion, Angle Class II
Methanesulfonate Sodium, Noramidopyrine
Neoplasm, Thymus
Neoplasms, Thymus
Neurobion
Neuroepitheliomas
Newborn Hemolytic Disease
Newborn Hemolytic Diseases
Noramidopyrine Methanesulfonate Sodium
Nutrition Disorder
Nutrition Disorders
Oculoauriculovertebral Syndrome
Ophthalmia Neonatorum
Osteolyses
Osteolysis
Osteomalacia
Pneumocystoses
Pneumonia, Interstitial Plasma Cell
Pneumonias, Pneumocystis carinii
Prostatic Hyperplasia
Pseudopregnancies
Psychomotor Agitation
Psychomotor Excitement
Purpura, Autoimmune Thrombocytopenic
Purpura, Idiopathic Thrombocytopenic
Purpura, Thrombocytopenic, Autoimmune
Purpura, Thrombocytopenic, Idiopathic
Purpuras, Autoimmune Thrombocytopenic
Purpuras, Idiopathic Thrombocytopenic
Rachitides
Reflex, Babinski
Reflexes, Babinski
Restlessness
Self Destructive Behavior
Sonifilan
Stasis Ulcer
Stasis Ulcers
Sterility
Suppuration
Syndrome, De Toni-Debre-Fanconi
Syndrome, Goldenhar
Syndrome, Hyper-IgE
Syndrome, Oculoauriculovertebral
Syndrome, Twin Transfusion
Syndrome, Waardenburg's
Syndromes, Twin Transfusion
Tetanus Toxoid
Thrombocytopenic Purpura, Idiopathic
Thrombocytopenic Purpuras, Idiopathic
Thymus Neoplasm
Thymus Neoplasms
Toxoid, Tetanus
Transfusion Syndrome, Twin
Transfusion Syndromes, Twin
Transfusion, Fetofetal
Transfusion, Twin
Transfusions, Fetofetal
Transfusions, Twin
Tuberculoses, Bone
Twin Transfusion
Twin Transfusion Syndrome
Twin Transfusion Syndromes
Twin Transfusions
Ulcers, Stasis
Vaccine, Di-Te-Per
Vaccine, Diphtheria-Pertussis-Tetanus
Vaccine, Diphtheria-Tetanus-Pertussis
Vaccine, DPT
Vaccine, DTP
Verrucas
Waardenburgs Syndrome
Warts
Werlhof Disease
Werlhof's Disease
Werlhofs Disease
1-hydroxy-3-aminopropane-1,1-diphosphonic acid
2,6-dichlorobenzaldehyde, (4-amino-4H-1,2,4-triazol-3-yl)hydrazone
3,5,9-Trioxa-4-phosphapentacosan-1-aminium, 4-hydroxy-N,N,N-trimethyl-10-oxo-7-((1-oxohexadecyl)oxy)-, hydroxide, inner salt, 4-oxide, (R)-, mixt. with formaldehyde polymer with oxirane and 4-(1,1,3,3-tetramethylbutyl)phenol, and 1-hexadecanol
3-(hydroxymethyl)-1-(((5-nitro-2-furanyl)methylene)amino)- 2,4-imidazolidinedione
3-hydroxymethylnitrofurantoin
4-piperidinecarboxylic acid, 1-(3-cyano-3,3-diphenylpropyl)-4-phenyl-, ethyl ester, monohydrochloride, mixt. with endo-(+-)-8-methyl-8-azabicyclo(3.2.1)oct-3-yl alpha-(hydroxymethyl)benzeneacetate sulfate (2:1) (salt)
Acetamide, N-(1-(2-(4-ethyl-4,5-dihydro-5-oxo-1H-tetrazol-1-yl)ethyl)-3-methyl-4-piperidinyl)-N-(2-fluorophenyl)-2-methoxy-, monohydrochloride, cis-(+-)-
AL 721
ampicillin-dicloxacillin mixture
benzenesulfonamide, 4-amino-N-2-pyrimidinyl-, mixt. with 5-((3,4,5-trimethoxyphenyl)methyl)-2,4-pyrimidinediamine
bolandiol dipropionate
carob
carob bean gum
carob flour
co-tetroxazine
cotetroxazine
D-gluconic acid
estr-4-ene-3 beta,17 beta-diol dipropionate
FSH-beta
glucaron
gluconic acid
isotonil
istonil
locust bean gum
nifurtoinol
omniderm
phenylalanine hydroxylase cofactor
Pregna-1,4-diene-3,20-dione, 9-fluoro-11-hydroxy-16-methyl-17,21-bis(1-oxopropoxy)-, (11beta,16beta)-, mixt. with 2-hydroxybenzoic acid
sulfadiazine-trimethoprim mixture
supercol
thiophene-2-carboxylic acid
trimethoprim-sulfadiazine mixture
UCB-630
Disease, Werlhof's
Syndrome, Guerin-Stern
Syndrome, Guillain-Barre
Syndrome, Job's
6R-BH4
1,2-Ethanediamine, N,N-dimethyl-N'-(3-pyridinylmethyl)-N'-(4-(2,4,6-tris(1-methylethyl)phenyl)-2-thiazolyl)-
Mixed Tumor, Mesodermal
Mesodermal Mixed Tumors
Mixed Tumors, Mesodermal
Tumor, Mesodermal Mixed
Tumors, Mesodermal Mixed
Mesothelial Neoplasms
Neoplasms, Mesothelial
Mesothelial Neoplasm
Neoplasm, Mesothelial
Blockers, Ganglionic
Bromide, Glycopyrronium
Ganglionic Blockers
Guillain Barre Syndrome
Mesodermal Mixed Tumor
Rheumatoid Arthritis, Juvenile
Separation Anxiety
Tuberculosis, Bone
Ulcer, Stasis
Wart
1,2-Benzenediol, 4,4'-(2,3-dimethyl-1,4-butanediyl)bis-
Benzeneacetic acid, alpha-(hydroxymethyl)-, 9-methyl-3-oxa-9-azatricyclo(3.3.1.02,4)non-7-yl ester, (7(S)-(1alpha,2beta,4beta,5alpha,7beta))-
L-Proline, 1-(N-(1-carboxy-3-phenylpropyl)-L-alanyl)-, dihydrate, (S)-
Pregna-1,4-diene-3,20-dione, 9-fluoro-11,21-dihydroxy-16-methyl-17-((1-oxopentyl)oxy)-, (11beta,16beta)-
Pyridinium, 3,3'-(1,6-hexanediylbis((methylimino)carbonyl)oxy)bis-1-methyl-, dibromide
Pyrrolidinium, 3-((cyclopentylhydroxyphenylacetyl)oxy)-1,1-dimethyl-, bromide
Sulfonium, (3-amino-3-carboxypropyl)dimethyl-, chloride, (S)-
fluocinolone-neomycin combination
Weakness
Ether
Alzheimer's Disease
Ethyl Ether
GnRH
Hyperthermia
Nordihydroguaiaretic Acid
Sulfonamides
Trisomy 21
AL-721
CPT 11
Decapeptyl
ESRD
Prion Disease
Neotigason
9-amino-20(S)-camptothecin
Discomfort
End Stage Kidney Disease
Phenothiazine
hypoglycemia
leukopenia
lymphosarcoma
tetanus toxoid
wart
metastatic cancer
Carboplat
DeCortin
Distention
Ergostat
Synvinolin
Grade 4
Temodal
Septisol
Anexate
oligodendroglioma
secondary tumor
AG3340
Intracerebral Hemorrhage
trichothiodystrophy
sterile
RDS
RPI.4610
mistletoe lectin
Suprecur
Myxofibrosarcoma
Follicular Variant Papillary Carcinoma
Human Papillomavirus 16 E6 Peptide
Madelung's Disease
Myxoid Malignant Fibrous Histiocytoma
Nasopharyngeal Keratinizing Squamous Cell Carcinoma
Thyroid Atrophy
Turban Tumor
Tubulin Interaction
Unknown Cellular or Molecular Interaction
Profact
Zentel
BCR Signaling Pathway
Camptothecin 11
1,1'-[1,4-Phenylenebis(methylene)]-bis-1,4,8,11-tetraazacyclotetradecane
9-Amino-20-(S)-camptothecin
Human Papillomavirus 16 E7 Peptide
Life Threatening Adverse Event
Lutex
Microcystic Changes
MoAb: Hu1D10
N-Debenzoyl-N-(tert-butoxycarbonyl)-10-deacetyltaxol
NDGA
Adenosine deaminase inhibitor
Nordihydroguaiaretic acid
Poly(I).Poly(c12,U)
Poly(Inosinic Acid) Poly(Cytidylic(12), Uridylic)Acid
Psyllium Husk
Riboazauracil
Aplidin
[2R-[2*(4R*,8R*)]]-3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-Benzopyran-6-ol acetate
rhGH
secondary cancer
Humanized Monoclonal Antibody LM609
Lu tex
Lanexat
Xylonest
Calcium Chloride Anhydrous
Standard Toxicity Grade 4
Sulindac Sulfoxide
Ancell-Spiegler Syndrome
Tetraisopropyl-2-(3,5-di-tert-butyl-4-hydroxyphenyl)ethylidene-1,1-diphosphonate
Teturamin
Thyroid Gland Atrophy
Tubulin Binding
U90
Unknown Cellular or Molecular Mechanism
Valvular Insufficiency
Valvular Regurgitation
Vitamin-D
BAY 43-9006 Tosylate
Benign Paraganglioma
Benign Paraganglionic Neoplasm
Bladder Distention
Blood Loss
CCRIS 5959
CTCAE Grade 4
Cholesterol Deposit
3,3',4',5,7-Pentahydroxyflavone
3,4-Dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-ol Acetate
Common Terminology Criteria for Adverse Events Grade 4
4,4'-(2,3-Dimethyl-1,4-butanediyl)bis[1,2-benzenediol]
DW 61
Dermadex
Drenusil
1,1'-Oxybisethane
End Stage Kidney Failure
End Stage Renal Failure
Epidermal Hyperplasia
Follicular Variant Papillary Thyroid Gland Carcinoma
Follicular Variant Thyroid Gland Papillary Carcinoma
Grade 4 Life Threatening or Disabling Adverse Event
Halichondrin B Analog
Hydantoin, 3-ethyl-5-phenyl-
I 124 MoAb cG250
I3A
ICI 176,334
Impaired Vision
Ingenol 3-Angelate
1,7-Dihydro-6H-purine-6-thione Monohydrate
Kalimin
Keratinizing Epidermoid Carcinoma of Nasopharynx
Keratinizing Epidermoid Carcinoma of the Nasopharynx
Keratinizing Squamous Cell Carcinoma of Nasopharynx
Keratinizing Squamous Cell Carcinoma of the Nasopharynx
Laryngeal Anaplastic Carcinoma
Laryngeal Giant Cell Carcinoma
Laryngeal Papillary Squamous Cell Carcinoma
Laryngeal Undifferentiated Carcinoma
Launois-Bensaude Syndrome
Life Threatening or Disabling Adverse Event
Loss Of Vision
Lung Overinflation
Macular Lesion
Madelung Disease
Mallory Bodies Present
Memory Dysfunction
Mestinon Bromide
Microcystic Change
Miltown 600
Acetic Acid, Zinc Salt, Dihydrate
N-[-4-[(3-Chloro-4-fluorophenyl)amino]-7-[3-(4-morpholinyl)propoxy]-6-quinazolinyl]-2-propenamide
NIH 10186
NIH 8805
Nasopharyngeal Keratinizing Epidermoid Carcinoma
Naturon
Opiran
PEG-3350 and electrolytes for oral solution
Parenchymatous Hemorrhage
Primary Cutaneous Diffuse Large B-Cell Lymphoma
Primary Lymphedema
Primary Splenic Diffuse Large B-Cell Lymphoma
Primary Splenic Follicular Lymphoma
Proftril
Psyllium Seed Husk
RG1068
RX 6029-M HCl
Regonal
Right Ventricular Failure
SDZ-ENA 713
SK&F 101468-A
Seresta
Skin Erosion
Spasmal
Eye finding
IRMA - Intraretinal microvascular abnormality
Monoethanolamine oleate
Pamidronic acid
Fetus, Mummified
X-Linked Severe Combined Immunodeficiency
American Pharmaceutical Brand of Vasopressin
American Regent Brand of Vasopressin
Beaufour Brand of Triptorelin Embonate
Beaufour Brand of Triptorelin
CVT-E002
Chemoautotrophy
Chemolithotrophy
Citanest Octapressin
Decapeptyl Depot
Decapeptyl LP
Decapeptyl Trimestral
Dengue Vaccines
Ferring Brand of Triptorelin Acetate
Ipsen Brand of Triptorelin Embonate
Ipsen Brand of Triptorelin
Nalbuphine Serb
SERB brand of nalbuphine
Serb, Nalbuphine
Trimestral, Decapeptyl
Triptorelin Beaufour Brand
Triptorelin Ipsen Brand
Vaccines, Dengue
X Linked Severe Combined Immunodeficiency
indacaterol
lovastatin-niacin combination
nalbuphine SERB brand
terutroban
paliperidone
N-(4-(3-amino-1H-indazol-4-yl)phenyl)-N1-(2-fluoro-5-methylphenyl)urea
Feces: blood
Nephrogenic systemic fibrosis
Delusion of pregnancy
Dental disorder
Passage of bloody stools
Raspberry leaf
Blood in feces
Psychological pseudocyesis
Phantom pregnancy
Restlessness behavior
ALDOSTERONE DEFICIENCY II
PROSOPAGNOSIA, CONGENITAL
Hypoglycemia
Hiatal hernia
Visual loss
Abnormal isoelectric focusing of serum transferrin (type I pattern)
CDG Il
Sinus arrest
MYOTONIA CONGENITA, ATYPICAL
Severe progression
USH2C
FHD
OMENN SYNDROME
MYOTONIC MYOPATHY, PROXIMAL
PHHI
HYPERINSULINISM, NEONATAL
HYPERINSULINISM, CONGENITAL
HYPERINSULINISM, FAMILIAL
Large for gestational age
MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa
NEUROFIBROMATOSIS WITH NOONAN PHENOTYPE
ALBINISM, BLACK LOCK, CELL MIGRATION DISORDER OF THE NEUROCYTES OF THE GUT, AND DEAFNESS
MSTD
SPONDYLOEPIPHYSEAL DYSPLASIA, LATE
CIDX
Increased blood ammonia
HYPERGONADOTROPIC OVARIAN FAILURE, X-LINKED
NBM1
Large head circumference
FITZSIMMONS SYNDROME
EPSTEIN-BARR VIRUS INFECTION, FAMILIAL FATAL
CARDIOMYOPATHY, DILATED, 3B
SCIDX1
XSCID
AHCH
OFCD SYNDROME
BRONZE SCHILDER DISEASE
MENTAL RETARDATION, X-LINKED, HYDE-FORSTER TYPE
OFD6
ORAL-FACIAL-DIGITAL SYNDROME, TYPE VI
Hepatocellular carcinoma
GRTH
DOLICHOSPONDYLIC DYSPLASIA
SULFITE OXIDASE DEFICIENCY
NANA STORAGE DISEASE
Thin nares
Increased serum ferritin level
PYRUVATE KINASE DEFICIENCY OF RED CELLS
POTASSIUM AND MAGNESIUM DEPLETION
FOLLING DISEASE
CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY
AT-V1
MECKEL SYNDROME, TYPE 1
MAPLE SYRUP URINE DISEASE, TYPE IB
MSUD3
Intrauterine growth failure
ICHTHYOSIS CONGENITA
IMMUNOGLOBULIN DEFICIENCY, LATE-ONSET
HYPERLIPOPROTEINEMIA, TYPE IA
Malpositioned teeth
AMISH BRITTLE HAIR BRAIN SYNDROME
ODG1
OVARIAN FAILURE, HYPERGONADOTROPIC
EPIDERMOLYSIS BULLOSA JUNCTIONALIS, PROGRESSIVE
'De Toni-Fanconi-Debre' syndrome
CYSTINOSIS, NEPHROPATHIC
HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA
DYSSYNERGIA CEREBELLARIS MYOCLONICA OF HUNT
CARNOSINASE DEFICIENCY
CDG IIa
BRONCHOMALACIA
Class II malocclusion
BLS
ANIRIDIA, CEREBELLAR ATAXIA, AND MENTAL DEFICIENCY
AMAUROSIS CONGENITA OF LEBER I
RETINAL BLINDNESS, CONGENITAL
DELTA STORAGE POOL DISEASE
ACYL-CoA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF
ADVIRC
TRACHEOPATHIA OSTEOPLASTICA
STUT1
SED CONGENITA
FSP1
Posterior urethral valves
Ovarian sex cord tumors
POLYDACTYLY, POSTAXIAL, TYPE A1
Bullae
Astrogliosis
Hyperimidodipeptiduria
MARBLE BONES, AUTOSOMAL DOMINANT
OSTEOSCLEROSIS FRAGILIS GENERALISATA
LEUKOPENIA, BENIGN FAMILIAL
IGAN
LANDOUZY-DEJERINE MUSCULAR DYSTROPHY
Sebaceous adenomas
FAMMM
MACULAR DEGENERATION, SENILE
MACULAR DYSTROPHY, VITELLIFORM
MCL
HYPERCALCEMIA, FAMILIAL BENIGN
PALMOPLANTAR KERATODERMA, VORNER TYPE
Positive Ortolani sign
GLM
IMMUNOGLOBULIN A, SELECTIVE DEFICIENCY OF
MODY2
CLEFT PALATE
HEPATIC DUCTULAR HYPOPLASIA, SYNDROMATIC
CMT1E
CRC
STICKLER SYNDROME, VITREOUS TYPE 1
STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE
AMC
ANEMIA, CONGENITAL ERYTHROID HYPOPLASTIC
BBBG1
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic
NPC1
IRAN, TYPE A
LENTIGINOSIS, GENERALIZED
CDGIl
Aqueduct of Sylvius stenosis
Hyperelastic skin
Vertebral compression fractures
AICARDI-GOUTIERES SYNDROME 2
Limb-girdle muscle weakness
Trunk hypotonia
Retrocollis
Inability to sit unsupported
CDG IIe
CDGIIe
Spondyloepiphyseal dysplasia
MYOTONIA, POTASSIUM-AGGRAVATED
SODIUM CHANNEL MUSCLE DISEASE
MYOTONIA CONGENITA, ACETAZOLAMIDE-RESPONSIVE
Wide ribs
Renal cysts
Impaired renal function
Dental crowding
Hyperinsulinism
Joint hypermobility
SOLDIERS HEART
Renal dysplasia
HDLD
FAMILIAL HDL DEFICIENCY
GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 1
BILE DUCT CYSTS
DM2
Short stature, severe disproportionate
HHF2
Balance impairment
NEUROFIBROMATOSIS-NOONAN SYNDROME
PALLIDOPONTONIGRAL DEGENERATION
atrioventricular septal defect
Wide nasal bridge
PREMATURE OVARIAN FAILURE, X-LINKED
CSNB, COMPLETE, X-LINKED
HHA
INCONTINENTIA PIGMENTI
BLOCH-SULZBERGER SYNDROME
XLP
IMMUNODEFICIENCY 5
Factor VIII deficiency
Asymmetric skull
Infantile spasms
CMD3B
SCIDX
ADDISON DISEASE AND CEREBRAL SCLEROSIS
THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL RECESSIVE
LE MERRER SYNDROME
Adrenal gland agenesis
Increased head circumference
SPG17
NSD
TIBIA VARA
BLOUNT DISEASE
Tethered cord
NIEMANN-PICK DISEASE, SUBACUTE JUVENILE FORM
SIALIDOSIS, TYPE II
Prenatal onset growth retardation
HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1
Rapid progression
MUSCULAR ATROPHY, SPINAL, INTERMEDIATE TYPE
SEEMANOVA SYNDROME II
MKS
DYSENCEPHALIA SPLANCHNOCYSTICA
IMMUNE DEFECT DUE TO ABSENCE OF THYMUS
ICHTHYOSIS CONGENITA II
ADDISON DISEASE
HYPERCHYLOMICRONEMIA, FAMILIAL
HAIR-BRAIN SYNDROME
GONADAL DYSGENESIS, XX TYPE
CARDIOMEGALIA GLYCOGENICA DIFFUSA
Rhizomelic dwarfism
FANCONI-BICKEL SYNDROME
EPIDERMOLYSIS BULLOSA JUNCTIONALIS, DISENTIS TYPE
ED4
CTNS
RESISTANCE TO THYROTROPIN
CACD
HEM SKELETAL DYSPLASIA
CPD5
ATYPICAL MYCOBACTERIOSIS, FAMILIAL
SCID, HLA CLASS II-NEGATIVE
GLYCOSYLASPARAGINASE DEFICIENCY
LCA1
ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE
ELEJALDE SYNDROME
SCHINZEL ACROCALLOSAL SYNDROME
VENTRICULAR HYPERTROPHY, HEREDITARY
ECTOPIC ERUPTION OF TEETH
SPLIT-HAND/FOOT MALFORMATION 1
SPLIT-HAND DEFORMITY
SDSEM
Ocular motor apraxia
Right ventricular failure
PBGD DEFICIENCY
ADENOMATOUS POLYPOSIS COLI, ATTENUATED
OIC
NEUTROPENIA, CHRONIC FAMILIAL
Sebaceous gland hyperplasia
Nevi
Secundum atrial septal defect
MELANOMA, MALIGNANT
LENTIGINOSIS, DIFFUSE
LEIOMYOMA, MULTIPLE CUTANEOUS
Scapulae exostoses
HYPERKERATOSIS, LOCALIZED EPIDERMOLYTIC
Psychomotor agitation
MNG1
CEMENTAL DYSPLASIA, PERIAPICAL
FACIAL HEMIHYPERTROPHY
ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN
ECTOPIA LENTIS, FAMILIAL
DUANE RETRACTION SYNDROME 1
DGI1
Agenesis of teeth
Displaced teeth
CAVERNOUS ANGIOMA, FAMILIAL
CAVERNOUS ANGIOMATOUS MALFORMATIONS
CAM
P2(k) PHENOTYPE
Dilated cerebral ventricles
SPDA1
BDS
AREGENERATIVE ANEMIA, CHRONIC CONGENITAL
AASE SYNDROME
ACROCEPHALOSYNDACTYLY, TYPE II
DEMENTIA, FRONTOTEMPORAL, WITH PARKINSONISM
MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL
INSULIN RECEPTOR, DEFECT IN, WITH INSULIN-RESISTANT DIABETES MELLITUS AND ACANTHOSIS NIGRICANS
AGS2
Facial asymmetry
Impaired balance
FVS
Depression
Trunk ataxia
TRIFUNCTIONAL PROTEIN DEFICIENCY
Mandibular prognathism
Gastrointestinal infections
Lymph node hyperplasia
Sparse eyebrows
Clubbed hand
Fumaric aciduria
Chemodectomas
Emphysema
SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA
Vertebral endplate irregularity
Radial hypoplasia
Choreoathetosis, paroxysmal
HYPOMAGNESEMIA, INTESTINAL, WITH SECONDARY HYPOCALCEMIA
HYPERINSULINEMIC HYPOGLYCEMIA, PERSISTENT
Absent patellar reflexes
CMS2A
NEVO SYNDROME
NPHS2
PERONEAL MUSCULAR ATROPHY WITH PYRAMIDAL FEATURES, AUTOSOMAL DOMINANT
MULTIPLE SYSTEM TAUOPATHY WITH PRESENILE DEMENTIA
COMBINED IMMUNODEFICIENCY, X-LINKED
IMD6
SEEMANOVA SYNDROME I
CSNB1A
MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS
WEST SYNDROME, X-LINKED
LYMPHOPROLIFERATIVE DISEASE, X-LINKED
IMMUNODEFICIENCY, X-LINKED PROGRESSIVE COMBINED VARIABLE
Narrow auditory canals
SCID, X-LINKED
TRANSKETOLASE DEFECT
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1
CHNG1
GTHR
COLD-INDUCED SWEATING SYNDROME 1
CISS1
SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS
Rheumatoid arthritis, juvenile
PK DEFICIENCY
GLYCOGENOSIS OF LIVER AND MUSCLE, AUTOSOMAL RECESSIVE
PHENYLALANINE HYDROXYLASE DEFICIENCY
SANTAVUORI DISEASE
NEURAMINIDASE 1 DEFICIENCY
HHF1
NESIDIOBLASTOSIS OF PANCREAS
NEPHRONOPHTHISIS 1
NPH1
NECROTIZING ENCEPHALOPATHY, INFANTILE SUBACUTE, OF LEIGH
ARSA DEFICIENCY
BRIC1
SUMMERSKILL SYNDROME
COLLODION FETUS
HYPOGAMMAGLOBULINEMIA, ACQUIRED
LYSINE:ALPHA-KETOGLUTARATE REDUCTASE DEFICIENCY
TRICHOTHIODYSTROPHY, NONPHOTOSENSITIVE 1
GAUCHER DISEASE, NONCEREBRAL JUVENILE
HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY
GLYCOGENOSIS, FANCONI TYPE
GABEB
Decreased taste
CHOROIDAL SCLEROSIS
CARNOSINEMIA
BARE LYMPHOCYTE SYNDROME, TYPE II
SEVERE COMBINED IMMUNODEFICIENCY, HLA CLASS II-NEGATIVE
ONDINE-HIRSCHSPRUNG DISEASE
TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME
MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES
ADULT NEURONAL CEROID LIPOFUSCINOSIS
SPIELMEYER-SJOGREN DISEASE
AMDH
ACROMESOMELIC DWARFISM
ACROCEPHALOPOLYDACTYLOUS DYSPLASIA
Tics
SPONDYLOEPIPHYSEAL DYSPLASIA, CONGENITAL TYPE
SHFD1
ECTRODACTYLY
ECD
OLIVOPONTOCEREBELLAR ATROPHY, HOLGUIN TYPE
OPCA2
RIEG
GIGANTISM, PARTIAL, OF HANDS AND FEET, NEVI, HEMIHYPERTROPHY, AND MACROCEPHALY
'HAPSBURG JAW'
PORPHYRIA, SWEDISH TYPE
UPS DEFICIENCY
AAPC
ADYNAMIA EPISODICA HEREDITARIA WITH OR WITHOUT MYOTONIA
OSTEOGENESIS IMPERFECTA CONGENITA, PERINATAL LETHAL FORM
HEMIFACIAL MICROSOMIA
THD
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A
FSHD1A
Sebaceous epitheliomas
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
VMD
VITELLIFORM MACULAR DYSTROPHY, EARLY-ONSET
BEST MACULAR DYSTROPHY
MACULAR DEGENERATION, POLYMORPHIC VITELLINE
Juvenile glaucoma
Hyposmia
LENTIGINOSIS PROFUSA
PUJO
HSCR1
CEMENTOMAS, FAMILIAL MULTIPLE
MSSE
DPD1
EOTD
DEFN
CROUZON SYNDROME
Chorioretinal atrophy
Renal cyst
CARDIAC CONDUCTION DEFECT, PROGRESSIVE
BRANCHIOOTORENAL DYSPLASIA
ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE
MYOADENYLATE DEAMINASE DEFICIENCY, MYOPATHY DUE TO
AAA1
PSEUDO-PHLORIZIN DIABETES
HIGH DENSITY LIPOPROTEIN DEFICIENCY
ENO4
Malrotation of the gut
Intracerebral hemorrhage
DIABETES MELLITUS, INSULIN-RESISTANT, WITH ACANTHOSIS NIGRICANS
PROSOPAGNOSIA, HEREDITARY
FACE BLINDNESS
Behavioral problems
Macroglossia
CCA4
Exercise intolerance
Irregular vertebral endplates
Absent kidney
Prenatal growth retardation
LCHAD DEFICIENCY
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I
Lipid accumulation
Congenital fibrosis of extraocular muscles
USHER SYNDROME, TYPE IIC
HYPOCERULOPLASMINEMIA
RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA
FSGS1
HOMOCYSTEINEMIA
CDG Ic
HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 2
Small scrotum
BFIS1
CMS IIa
Curly hair
GALLBLADDER DISEASE 1
Lumbar disk herniation
PUERTO RICAN INFANT HYPOTONIA SYNDROME
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED
HEMERALOPIA-MYOPIA
INCONTINENTIA PIGMENTI, TYPE II, FORMERLY
XLPD
DUNCAN DISEASE
IMD5
PURTILO SYNDROME
Prenatal growth deficiency
CCT
Skeletal myopathy
CARDIOMYOPATHY, DILATED, X-LINKED
OCULOFACIOCARDIODENTAL SYNDROME
AMN
MELANODERMIC LEUKODYSTROPHY
OPITZ SYNDROME, X-LINKED
OGS1
THYROTROPIN RESISTANCE
TSH RESISTANCE
HYPOTHYROIDISM, CONGENITAL, DUE TO TSH RESISTANCE
HYPOSPLENIA, ISOLATED CONGENITAL
SILVER SPASTIC PARAPLEGIA SYNDROME
SIALURIA, FRENCH TYPE
Right ventricular outlet obstruction
INFLAMMATORY BOWEL DISEASE 1
IBD1
Arthrogryposis multiplex congenita
Fusion of cervical vertebrae
PHENYLKETONURIA
OLIGOPHRENIA PHENYLPYRUVICA
NEU1 DEFICIENCY
Stillborn
NPHP1
SNE
MYXOMA, INTRACARDIAC
MYOPATHY, CONGENITAL
CARNITINE PALMITOYLTRANSFERASE IA DEFICIENCY
MUSCULAR DYSTROPHY, CONGENITAL, WITH CENTRAL NERVOUS SYSTEM INVOLVEMENT
Hypoplasia of choroid
Acetabular dysplasia
MOYAMOYA DISEASE 1
MOYAMOYA DISEASE
Hepatocellular necrosis
MICROCEPHALY WITH NORMAL INTELLIGENCE, IMMUNODEFICIENCY, AND LYMPHORETICULAR MALIGNANCIES
NADPH-DEPENDENT METHEMOGLOBIN REDUCTASE DEFICIENCY
MECKEL-GRUBER SYNDROME, TYPE 1
MECKEL-GRUBER SYNDROME
MSUD1B
ADRENAL HYPOPLASIA
Duplicated ureter
Visual defects
ACHALASIA-ALACRIMA SYNDROME
GERMAN SYNDROME
EPIDERMOLYSIS BULLOSA JUNCTIONALIS, SEVERE NONLETHAL
CLPED1
DOOR SYNDROME
CYSTINOSIN, DEFECT OF
CYSTINOSIS, INFANTILE NEPHROPATHIC
CYSTATHIONASE DEFICIENCY
TRUNCUS ARTERIOSUS COMMUNIS
CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE
Decreased thyroxine
Pigmented nevi
BARE LYMPHOCYTE SYNDROME
HYPOTRANSFERRINEMIA, FAMILIAL
ASPARTYLGLUCOSAMINIDASE DEFICIENCY
Elbow ankylosis
NEURONAL CEROID LIPOFUSCINOSIS, JUVENILE
Mood disturbances
THYROGLOSSAL DUCT CYST, FAMILIAL
IDIOPATHIC THROMBOCYTOPENIC PURPURA
ITP
Tarsal fusions
STAMMERING
SEDC
FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1
RGS
RETICULAR PIGMENT ANOMALY OF FLEXURES
RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL DOMINANT
NAIT
GLOMUS TUMORS, FAMILIAL, 1
VROLIK TYPE OF OSTEOGENESIS IMPERFECTA
Branchial cleft remnant
BERGER DISEASE
MYOTONIA CONGENITA, AUTOSOMAL DOMINANT
Muscle weakness, limb-girdle
LIPOMATOSIS, MULTIPLE
LENTIGINOSIS, INHERITED PATTERNED
MCUL1
'DOUBLE TOOTH'
HERNIA, HIATUS
Hawkinsinuria
HAIRY ELBOWS
GBS
GIGANTIFORM CEMENTOMA, FAMILIAL
MENETRIER DISEASE
GAMSTORP-WOHLFART SYNDROME
IGAD1
GAMMA-A-GLOBULIN, SELECTIVE DEFICIENCY OF
LUDER-SHELDON SYNDROME
POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL
ENOLASE, SPERM SPECIFIC
'Chocolate' cysts of ovary
MODY, GLUCOKINASE-RELATED
DENTINOGENESIS IMPERFECTA WITHOUT OSTEOGENESIS IMPERFECTA
OPALESCENT TEETH WITHOUT OSTEOGENESIS IMPERFECTA
DANUBIAN ENDEMIC FAMILIAL NEPHROPATHY
CRANIOFACIAL DYSOSTOSIS, TYPE I
CEREBRAL CAVERNOUS MALFORMATIONS
PCCD
P1(k) PHENOTYPE
STL1
ANORECTAL ANOMALIES
SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1
NEUROFIBROMATOSIS, CENTRAL TYPE
ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE
PROSOPAGNOSIA, DEVELOPMENTAL
Cranium bifidum
Eye deviation
Spastic quadriparesis
Impaired vision
Metatarsus adductus
DFSP
GIANT CELL FIBROBLASTOMA
Thickened helices
Diminished muscle strength
ORTHOSTATIC INTOLERANCE
IRRITABLE HEART
CERVICAL CANCER
CLE
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1
CDGIc
Malabsorption
RICKER SYNDROME
PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY
Selective IgA deficiency
NFNS
Aqueductal stenosis
BRACHYDACTYLY-MENTAL RETARDATION SYNDROME
Normal blood pressure
Stippled epiphyses
SEDT
SED TARDA, X-LINKED
POF1
POF
Cerebellar abnormalities
Porencephaly
Rib hypoplasia
Hiatus hernia
BARAITSER SYNDROME
SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED
OPITZ-G SYNDROME, TYPE I
OPITZ BBBG SYNDROME, TYPE I
HYPOTHYROIDISM DUE TO UNRESPONSIVENESS TO THYROTROPIN
ASPLENIA, FAMILIAL
SPASTIC PARAPLEGIA 17
PYRUVATE KINASE DEFICIENCY OF ERYTHROCYTE
Cerebral hemorrhage
Absent upper lateral incisors
SACCADE INITIATION FAILURE, CONGENITAL
NEU DEFICIENCY
HYPOGLYCEMIA, HYPERINSULINEMIC, OF INFANCY
HYPERINSULINISM, FAMILIAL, WITH PANCREATIC NESIDIOBLASTOSIS
CPT DEFICIENCY, HEPATIC, TYPE I
Thickened ribs
ATAXIA-TELANGIECTASIA VARIANT V1
NONSYNDROMAL MICROCEPHALY, AUTOSOMAL RECESSIVE, WITH NORMAL INTELLIGENCE
METHEMOGLOBIN REDUCTASE DEFICIENCY
TPNH-METHEMOGLOBIN REDUCTASE DEFICIENCY
ARYLSULFATASE A DEFICIENCY
Bulbar palsies
Low parathyroid hormone
ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE
ABHS
BIDS SYNDROME
OVARIAN DYSGENESIS, HYPERGONADOTROPIC, WITH NORMAL KARYOTYPE
XX GONADAL DYSGENESIS
Amylo-1,6-glucosidase deficiency
FBS
FACIOTHORACOGENITAL SYNDROME
Equinovarus deformity
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa
CDGIIa
BLS, TYPE II
ATRANSFERRINEMIA
KUFS DISEASE
CEROID LIPOFUSCINOSIS, NEURONAL, 3
CLN3
PSEUDOHYPOPARATHYROIDISM, TYPE II
Interstitial pulmonary fibrosis
RENAL AGENESIS
Tarsal fusion
SPLIT-HAND/FOOT DEFORMITY 1
SHSF1
SPINOCEREBELLAR ATROPHY II
SPINOCEREBELLAR ATAXIA, CUBAN TYPE
STRUMPELL DISEASE
RIEG1
POIKILODERMA, HEREDITARY ACROKERATOTIC
PARAMYOTONIA CONGENITA OF VON EULENBURG
HFM
IGAN1
NEPHRITIS, IgA TYPE
MYOPATHY, FAMILIAL IDIOPATHIC INFLAMMATORY
BARLOW SYNDROME
Porencephalic cyst
DNS
MACULOPATHY, AGE-RELATED, 2
MSL
THANATOPHORIC DYSPLASIA, LUTON VARIANT
Idiopathic thrombocytopenic purpura
FHH1
KERATOSIS PALMARIS ET PLANTARIS FAMILIARIS
HYPERCHOLESTEROLEMIA, FAMILIAL, DUE TO LIGAND-DEFECTIVE APOLIPOPROTEIN B
STERNAL NONUNION WITH SUPRAUMBILICAL RAPHE
POLYNEUROPATHY, INFLAMMATORY DEMYELINATING, ACUTE
AIDP
GASTRITIS, FAMILIAL GIANT HYPERTROPHIC
MYOKYMIA, MYOTONIA, MUSCLE WASTING, AND HYPERHIDROSIS
FACTOR VIII DEFICIENCY
CYLINDROMATOSIS, FAMILIAL
Peritoneal inflammation
DURS1
DENTINOGENESIS IMPERFECTA, SHIELDS TYPE II
CAPDEPONT TEETH
Narrow, high-arched palate
Medullary cystic disease
CCM
STICKLER SYNDROME, TYPE I
CONGENITAL DEFECT OF SKULL AND SCALP
MARIE-STRUMPELL SPONDYLITIS
BLACKFAN-DIAMOND SYNDROME
Cerebrospinal fluid (CSF) with increased protein
Macular dystrophy
Protrusio acetabulae
CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY
STEROID 18-OXIDASE DEFICIENCY
Oculomotor apraxia
External auditory canal atresia
Loss of vision
LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY
MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe
Palatal tremor
MYOTONIA PERMANENS
DERMATOFIBROSARCOMA PROTUBERANS
Oligodontia
SPINOCEREBELLAR ATAXIA 22
Abnormal pinnas
FUMARIC ACIDURIA
BLEPHAROSPASM, BENIGN ESSENTIAL
ENCEPHALOPATHY OF CHILDHOOD
DFNA22
ABDOMINAL OBESITY-METABOLIC SYNDROME
ST. HELENA DYSPLASIA
Oligodactyly
HYPOMAGNESEMIC TETANY
Dysplastic kidneys
Intestinal malrotation
Shell teeth
Astrocytosis
NSRD4
DISINHIBITION-DEMENTIA-PARKINSONISM-AMYOTROPHY COMPLEX
BULBOSPINAL NEURONOPATHY, X-LINKED RECESSIVE
XBSN
PREMATURE OVARIAN FAILURE 1
OVARIAN FAILURE, PREMATURE
MYOPIA-NIGHT BLINDNESS
Phosphaturia
Renal Fanconi syndrome
XLCM
MENTAL RETARDATION, X-LINKED, WITH CRANIOFACIAL DYSMORPHISM
DFN4
Hyperphosphaturia
Uremia
THYROID-STIMULATING HORMONE, RESISTANCE TO
HYPOTHYROIDISM, NONAUTOIMMUNE
THYROID HORMONE UNRESPONSIVENESS
REFETOFF SYNDROME
Tetra-amelia
MGCT
Large head
PAH DEFICIENCY
CROSS SYNDROME
OCULAR MOTOR APRAXIA
COMA
CPT I DEFICIENCY
MUSCULAR DYSTROPHY, CONGENITAL PROGRESSIVE, WITH MENTAL RETARDATION
MITOCHONDRIAL NADH DEHYDROGENASE COMPONENT OF COMPLEX I, DEFICIENCY OF
Methylmalonyl-CoA mutase deficiency
GRUBER SYNDROME
ADRENAL APLASIA
Small nails
GLUCOCEREBROSIDASE DEFICIENCY
GBA DEFICIENCY
GALACTORRHEA
Keratoglobus
GLYCOGEN STORAGE DISEASE XI
Irregular endplates
CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME
ECTODERMAL DYSPLASIA, MARGARITA ISLAND TYPE
MOTH-EATEN SKELETAL DYSPLASIA
Infantile spasm
KUFS DISEASE, AUTOSOMAL RECESSIVE
PHP II
HYPOFIBRINOGENEMIA, CONGENITAL
ACROOSTEOLYSIS, NEUROGENIC
HYPERTROPHIC SUBAORTIC STENOSIS, IDIOPATHIC
TRIPHALANGEAL THUMB, NONOPPOSABLE
STUTTERING, FAMILIAL PERSISTENT 1
SHFM1
SCAPULOPERONEAL SYNDROME, MYOPATHIC TYPE
RETINAL VENOUS BEADING
Mesenteric thrombosis
'HABSBURG JAW'
PORPHYRIA, SOUTH AFRICAN TYPE
PORPHOBILINOGEN DEAMINASE DEFICIENCY
UROPORPHYRINOGEN SYNTHASE DEFICIENCY
Colon diverticula
THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE
PMC
OPTA2
OI, TYPE II
OSTEOGENESIS IMPERFECTA CONGENITA
Low urine uric acid
PIGMENTED MOLES
THOMSEN DISEASE
IIM
FSHMD1A
MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A
MLM
LIPOMA
LIPODYSTROPHY, CEPHALOTHORACIC
PLSDL
INCISORS, FUSED MANDIBULAR
HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE I
FAMILIAL BENIGN HYPERCALCEMIA 1
Atrial septal defect (ostium secundum type)
MEGACOLON, AGANGLIONIC
GUILLAIN-BARRE SYNDROME, FAMILIAL
IMMUNOGLOBULIN A DEFICIENCY 1
IgA, SELECTIVE DEFICIENCY OF
KERATOSIS PALMOPLANTARIS TRANSGREDIENS ET PROGREDIENS
MYOCLONIC EPILEPSY WITH CHOREOATHETOSIS
CLEFT PALATE, ISOLATED
CPI
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E
HMSN I
Malrotation of gut
Satyr ear
SCID DUE TO ADA DEFICIENCY, LATE-ONSET
CMO II DEFICIENCY
DIABETES MELLITUS, INSULIN-RESISTANT, WITH ACANTHOSIS NIGRICANS, TYPE A
THIOPURINES, POOR METABOLISM OF
Scalp defect
Retrognathia
Neutropenia
Acroosteolysis of distal phalanges
Visual inattentiveness
Fused cervical vertebrae
Reactive airway disease
Spastic tetraparesis
Prenatal-onset growth retardation
Clitoral hypertrophy
CHOLEDOCHOCELE
NOONAN-NEUROFIBROMATOSIS SYNDROME
Rib anomalies
GBD1
Dyscalculia
ALBRIGHT HEREDITARY OSTEODYSTROPHY-LIKE SYNDROME
CHARCOT-MARIE-TOOTH NEUROPATHY WITH PYRAMIDAL FEATURES, AUTOSOMAL DOMINANT
PPND
Decreased vibration sense
Addison disease
Polysplenia
XCID
IMMUNODEFICIENCY 6
POFX
INCONTINENTIA PIGMENTI, FAMILIAL MALE-LETHAL TYPE
IP2, FORMERLY
Hypomineralization of enamel
Septic arthritis
Cervical vertebral fusion
Vertebral anomalies
OSX
POLYDACTYLY, CLEFT LIP/PALATE OR LINGUAL LUMP, AND PSYCHOMOTOR RETARDATION
Adrenal hypoplasia
RTSH
GLOOMY FACE SYNDROME
SULFOCYSTEINURIA
SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET
Rib fusion
LEIGH NECROTIZING ENCEPHALOPATHY DUE TO PYRUVATE CARBOXYLASE DEFICIENCY
LEIGH SYNDROME DUE TO PYRUVATE CARBOXYLASE DEFICIENCY
Anterior chamber anomalies
KRAMER SYNDROME
OCULOMOTOR APRAXIA, COGAN TYPE
NIEMANN-PICK DISEASE, TYPE C1
SIALIDASE DEFICIENCY
BATTEN-TURNER CONGENITAL MYOPATHY
MUSCULAR ATROPHY, SPINAL, INFANTILE CHRONIC FORM
MYMY1
MYMY
NADH:Q(1) OXIDOREDUCTASE DEFICIENCY
NADH-COENZYME Q REDUCTASE DEFICIENCY
Dysplastic kidney
MECKEL SYNDROME
Upturned nose tip
DESQUAMATION OF NEWBORN
ALPHA-AMINOADIPIC SEMIALDEHYDE SYNTHASE DEFICIENCY
L-LYSINE:NAD-OXIDO-REDUCTASE DEFICIENCY
CHYLOMICRONEMIA, FAMILIAL
CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO
TTDN1
OVARIAN DYSGENESIS, HYPERGONADOTROPIC, AUTOSOMAL RECESSIVE
XXGD
GESTATIONAL TROPHOBLASTIC DISEASE
ACID BETA-GLUCOSIDASE DEFICIENCY
FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE
ZLOTOGORA-OGUR SYNDROME
ECTODERMAL DYSPLASIA, TYPE 4
ECTODERMAL DYSPLASIA, CLEFT LIP AND PALATE, MENTAL RETARDATION, AND SYNDACTYLY
LYSOSOMAL CYSTINE TRANSPORT PROTEIN, DEFECT OF
OSMED
NANCE-INSLEY SYNDROME
NANCE-SWEENEY CHONDRODYSPLASIA
CDPR
CEREBELLOPARENCHYMAL DISORDER V
ATYPICAL MYCOBACTERIAL INFECTION, FAMILIAL DISSEMINATED
MYCOBACTERIAL DISEASE, MENDELIAN SUSCEPTIBILITY TO
MSMD
OHD
IVEMARK SYNDROME
AGA DEFICIENCY
JNCL
VOGT-SPIELMEYER DISEASE
ALBINISM WITH HEMORRHAGIC DIATHESIS AND PIGMENTED RETICULOENDOTHELIAL CELLS
AFIBRINOGENEMIA, CONGENITAL
CMH1
Craniosynostosis (metopic suture)
CUSHING SYMPHALANGISM
SUPRAVALVAR AORTIC STENOSIS, EISENBERG TYPE
SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA
GOLDBLATT SYNDROME
SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA
SPG3A
PPH1
PHT
FIBROCYSTIC PULMONARY DYSPLASIA
ALBERS-SCHONBERG DISEASE, AUTOSOMAL DOMINANT
Vertebral hypoplasia
VITELLIFORM MACULAR DYSTROPHY, JUVENILE-ONSET
MACROGLOSSIA
LIPO
Isolated growth hormone deficiency
FBH1
HIATAL HERNIA
GLAUCOMA, PRIMARY OPEN ANGLE, ADULT-ONSET
RFS
PFCP
DIAPHYSEAL DYSPLASIA 1, PROGRESSIVE
Absent ear lobes
DGI-II
NEPHROPATHIA EPIDEMICA
CFD1
Supranuclear gaze paralysis
Optic neuropathy
CEREBRAL CAPILLARY MALFORMATIONS
MELNICK-FRASER SYNDROME
MULTIPLE BASAL CELL NEVI, ODONTOGENIC KERATOCYSTS, AND SKELETAL ANOMALIES
MPB
AOM
HYD1
SECOND PREMOLARS AND THIRD MOLARS, ABSENCE OF
TOOTH AGENESIS, FAMILIAL
BECHTEREW SYNDROME
ANEMIA, CONGENITAL HYPOPLASTIC, OF BLACKFAN AND DIAMOND
RED CELL APLASIA, PURE, HEREDITARY
ERYTHROGENESIS IMPERFECTA
AASE-SMITH SYNDROME II
ADIE PUPIL
ACRORENAL SYNDROME
HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1
Recurrent fevers
FHHA1B
Ichthyosis
Increased erythrocyte sedimentation rate (ESR)
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il
Prominent chin
Shallow anterior chamber
Myelodysplasia
Visual impairment
Lymphadenopathy
Idiopathic thrombocytopenic purpura (ITP)
PARK11
Enlarged mandible
SCA22
Frontal lobe dementia
Knee flexion deformities
AOMS1
CREE LEUKOENCEPHALOPATHY
Hyperphosphatemia
Food intolerance
MYOTONIC DYSTROPHY 2
PROXIMAL MYOTONIC MYOPATHY
PROMM
DFNB4
CHARCOT-MARIE-TOOTH DISEASE WITH PYRAMIDAL FEATURES, AUTOSOMAL DOMINANT
FRONTOTEMPORAL DEMENTIA WITH PARKINSONISM
DDPAC
FTD-ALS
Hypophosphatemia
MITOCHONDRIAL CYTOPATHY
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A
NIGHT BLINDNESS, CONGENITAL STATIONARY, WITH MYOPIA
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1
XLP1
LYP
EBVS
Raised CRP
CLARK-BARAITSER SYNDROME
SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE
AHX
SIEMERLING-CREUTZFELDT DISEASE
LISSENCEPHALY AND AGENESIS OF CORPUS CALLOSUM
Ulceration
Skin erosions
SPLENIC HYPOPLASIA
SILVER SYNDROME
Stereotypical movements
NEURAMINIDASE DEFICIENCY
NEUG DEFICIENCY
HYPERINSULINEMIC HYPOGLYCEMIA DUE TO FOCAL ADENOMATOUS HYPERPLASIA
NEPHRONOPHTHISIS, FAMILIAL JUVENILE
SPONTANEOUS OCCLUSION OF THE CIRCLE OF WILLIS
IMMUNODEFICIENCY, MICROCEPHALY, AND CHROMOSOMAL INSTABILITY
CEREBROSIDE SULFATASE DEFICIENCY
MKS1
MES
Duplicated ureters
MANNOSIDOSIS, BETA A, LYSOSOMAL
Cytoplasmic vacuolization
LAMELLAR EXFOLIATION OF NEWBORN
ICR2
LIPD DEFICIENCY
HYPERBILIRUBINEMIA, SHUNT
OVARIAN DYSGENESIS 1
GLYCOGENOSIS, GENERALIZED, CARDIAC FORM
HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME
HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA
OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA
CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS
GREENBERG DYSPLASIA
SPINODENTATE ATROPHY
ATYPICAL MYCOBACTERIAL INFECTION, DISSEMINATED
OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES
CRB
NEUROPATHY, CONGENITAL SENSORY
THROMBOCYTOPENIC PURPURA, AUTOIMMUNE
HEREDITARY ABSENCE OF THE PROXIMAL INTERPHALANGEAL JOINTS
OLIVOPONTOCEREBELLAR ATROPHY II
SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT
SPG3
Self-destructive behavior
Capillary hemangiomas
PROGNATHISM, MANDIBULAR
PAPA
PIGMENTED PURPURIC ERUPTION
HOKPP
PARALYSIS PERIODICA PARAMYOTONICA
ENCHONDROMATOSIS, MULTIPLE
OSTEOCHONDROMATOSIS
Thickened stratum corneum
Cushing disease
Malposition of teeth
MACULAR DEGENERATION, AGE-RELATED, 2
ARMD2
BMD
Ph-positive acute lymphoblastic leukemia
PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE
KERATOSIS OF GREITHER
HYPERHEPARINEMIA
MGC
HAWKINSINURIA
OLIGODENDROGLIOMA
RENAL FANCONI SYNDROME
FANCONI SYNDROME WITHOUT CYSTINOSIS
ERYTHROCYTOSIS, FAMILIAL, 1
'TURBAN TUMOR' SYNDROME
ECTOPIA PUPILLAE
DENTINOGENESIS IMPERFECTA 1
OPALESCENT DENTIN
CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS
CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT
COLORECTAL CANCER
ARTHROGRYPOSIS MULTIPLEX CONGENITA
SCALP DEFECT, CONGENITAL
LUPUS ANTICOAGULANT, FAMILIAL
CRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA
BATTEN DISEASE
HHC1
Radial head dislocation/subluxation
Scanty hair
GANGLIONIC BLOCK AGENTS
POST TRANSLATIONAL AA MODIFICATION
NEOPL THYMUS
WERLHOF DIS
THER RELAT CANCER
ACUTE INFLAMM POLYRADICULONEUROPATHY
DEMYELINATING POLYRADICULONEUROPATHY ACUTE INFLAMM
INFLAMM POLYNEUROPATHY ACUTE
POLYNEUROPATHY ACUTE INFLAMM
JUVENILE PARKINSON DIS AUTOSOMAL RECESSIVE
HYPOXIC ISCHEMIC ENCEPH
ISCHEMIC HYPOXIC ENCEPH
ENCEPH HYPOXIC ISCHEMIC
AA MODIFICATION CO TRANSLATIONAL
BLOCK AGENTS GANGLIONIC
INFECT RESPIROVIRUS
AUTOSOMAL RECESSIVE JUVENILE PARKINSON DIS
BETA MANNOSIDASE DEFIC
CO TRANSLATIONAL PROTEIN MODIFICATION
PROTEIN PROC COTRANSLATIONAL
osemozotan
HEMOLYTIC DIS NEWBORN
DEFIC DIS GALACTOKINASE
GANGLIONIC BLOCK
INFECT
AA MODIFICATION POSTTRANSLATIONAL
THYMIC NEOPL
THER ASSOC CANCER
ADULT POLYCYSTIC KIDNEY DIS TYPE 2
NEOPL MESOTHELIAL
MESOTHELIAL NEOPL
POLYRADICULONEUROPATHY ACUTE INFLAMM DEMYELINATING
CO TRANSLATIONAL PROTEIN PROC
DEFIC GLUCOSEPHOSPHATE DEHYDROGENASE
NUTRITION DIS
PSEUDOPREGN
THYMUS NEOPL
POLYCYSTIC KIDNEY TYPE 2 AUTOSOMAL DOMINANT DIS
INFLAMM DEMYELINATING POLYRADICULONEUROPATHY ACUTE
FOURTH CRANIAL NERVE DIS
CO TRANSLATIONAL AA MODIFICATION
PROTEIN MODIFICATION COTRANSLATIONAL
silastic nomegestrol acetate
ENCEPH RUSSIAN SPRING SUMMER
GALACTOKINASE DEFIC DIS
NEOPL THYMIC
TREATMENT RELAT CANCER
ACUTE INFLAMM POLYNEUROPATHY
CRANIAL NERVE IV DIS
FAMILIAL PARKINSON DIS AUTOSOMAL RECESSIVE
GLUCOSEPHOSPHATE DEHYDROGENASE DEFIC
NUTRITIONAL DIS
RESPIROVIRUS INFECT
AA MODIFICATION POST TRANSLATIONAL
WERLHOFS DIS
PARKINSON DIS FAMILIAL AUTOSOMAL RECESSIVE
magnesium aluminosilicate
DEFIC GPD
POSTTRANSLATIONAL AA MODIFICATION
TREATMENT ASSOC CANCER
POLYRADICULONEUROPATHY ACUTE INFLAMM
RUSSIAN SPRING SUMMER ENCEPH
GPD DEFIC
ACUTE INFLAMM DEMYELINATING POLYRADICULONEUROPATHY
COTRANSLATIONAL PROTEIN PROC
TROCHLEAR NERVE DIS
Cyclin-Dependent Kinase Inhibitor AT7519M
Hyperacute Pancreatic Cancer Vaccine
Anti-CTLA4 Human Monoclonal Antibody CP-675,206
((R)-3-(5-(p-Fluorobenzyl)-2-thienyl)-1-methyl-2-propynyl-1-hydroxyurea
Beta-D-Glucopyranose
Blopress
2H-1,3,2-oxazaphosphorin-2-amine, N,N-is(2-chloroethyl)tetrahydro-,2-oxide
DTC
EPC2407
Giant Congenital Nevus
Growth Hormone Secretion Abnormality
Sterile
LAFB
Metal Chelating Agent
Viscum Album Extract
Arterenol
Jaw Osteonecrosis
TETRAZOLAST MEGLUMINE
Atreleuton
Atrioventricular Nodal Reentrant Tachycardia
Brain Astrocytoma
BW 64-9
Chelation
Ewing Family of Tumors
Sinoatrial Exit Block
Gluconic Acid
HYDROXYTOLUIC ACID
Hypotension
Isobutane
Left Anterior Hemiblock
Arquel
PELUBIPROFEN
Valeriana Officinalis Extract
RBBB
PVC
BIBW 2992
EGFR/HER2 TKI BIBW 2992
.BETA.-D-GLUCOPYRANOSE
Congenital Neutropenia
Fotretamine
2-Hydroxypropanoic Acid
Left Posterior Hemiblock
MORINAMIDE
Nail changes
ONJ
Pelubiprofen
VQD001
SSRT Agonist
Third Heart Sound
Weight Gain Adverse Event
PARGEVERINE
Second Degree AV Block
Second Degree Atrioventricular Block
Asparaginase-E.Coli
Chelating
Daily Smoker
L-m-Tyrosine
L-Phenylalanine, 3-hydroxy-
Lactic Acid, L-
Optic disc edema
Osteonecrosis of Jaw
Somatostatin Receptor Agonist
GONADORELIN
Hycamptamine
Vitamin D Compound
Premature Atrial Complex
Valerian
Paliperidone
cCLB8
Antiepileptics
Dual Tyrosine Kinase Inhibitor BIBW 2992
WIN 37284
N,N-Bis(2-chloroethyl)tetrahydro-2H-1,3,2-oxazaphosphorin-2-amine 2-Oxide
Death Adverse Event Not Associated with More Specific CTCAE Term NOS
Ewing's Sarcoma/Peripheral Primitive Neuroectodermal Tumor
Monoclonal Antibody IDEC-152
IRAMPANEL
Morinamide
Mucopolysaccharidosis Type IV
Peritoneal Hemorrhage Adverse Event
MKC-1
LDI-200
Vagina hemorrhage
Premature Ventricular Complex
ISOBUTANE
Neurosensory Disorder
Opioid Receptor Agonist
Intermittent AV Block
Ad-IFNg
Aminobenzoate
CNTO-328
Betiatide
Current Every Day Smoker
Current Smoker
Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor
FOTRETAMINE
hyperthermia
Hypotension Adverse Event
Metastatic Disease
Morquio Syndrome
Nail Changes Adverse Event
Shark Cartilage Extract AE-941
Pseudomembrane Formation
Short stature
Sinus Arrest/Pause
Vagina Hemorrhage Adverse Event
VPC
Weight gain
Sinus Pause
Monoclonal Antibody HGS-ETR2
(R)-1-(4-(4-Fluoro-2-methyl-1H-indol-5-yloxy)-5- methylpyrrolo[2,1-f][1,2,4]triazin-6-yloxy)propan- 2-ol
BETIATIDE
Dextrose Monohydrate
DEXTROSE MONOHYDRATE
Hydroxytoluic Acid
Irampanel
Large Cell Salivary Gland Carcinoma
Metal Chelator
Metal Chelant
Viscum album Extract
Mood Alteration
Pamidronic Acid
Pargeverine
Short Stature Adverse Event
Tetrazolast Meglumine
EGFR/HER2 Inhibitor AV-412
Antiepileptic Agent
Kostmann Disease
Every Day Smoker
HPV-16 E6 Peptide
LACTIC ACID, L-
Milk Acid
Anti-TRAIL Receptor 2 Monoclonal Antibody HGS-ETR2
Noradrenaline
Omenn Syndrome
Optic Disc Edema Adverse Event
Ovarian Serous Adenocarcinofibroma
PSA-PAH1
PALIPERIDONE
Palpitations Adverse Event
Palpitations
TS-1
Sinus Arrest
VALERIAN
D Vitamin
Lymphatic Sarcoma
Fujisawa Brand of Theophylline Sodium Glycinate
theo von ct
Pharmachem Brand of Triclosan
Triclosan Pharmachem Brand
Reckitt Brand of Triclosan
Asid Bonz Brand of Tripelennamine Hydrochloride
Ulcers, Venous Stasis
Reversible Posterior Leukoencephalopathy Syndrome
Lissencephalia
Lissencephalias
Neonatal Thrombocytopenia
Thrombocytopenia, Neonatal
Boro Scopol
von ct, theo
Bomathal
Pharmtech Brand of Thiopental Sodium
Swarm Brand of Thymol
Alloimmune Thrombocytopenias, Neonatal
staurosporinone
Diffuse Lymphoma
Sarcoma, Lymphatic
Boro-Scopol
ct Arzneimittel Brand of Theophylline Sodium Glycinate
Tilidin Godecke
Godecke, Tilidin
Progro T S
Stasis Ulcer, Venous
Stasis Ulcers, Venous
Thrombocytopenia, Neonatal Alloimmune
Lymphatic Sarcomas
Aerobin
Fameasan Brand of Theophylline Sodium Glycinate
ct, theo von
Pro Beef Brand of Trenbolone Acetate
Cliniclean
Venous Stasis Ulcer
Brain Cavernous Hemangiomas
Agyrias
Neonatal Thrombocytopenias
Thrombocytopenias, Neonatal
Thrombin Jones Brand
Sarcomas, Lymphatic
Lymphosarcomas
BoroScopol
Winzer Brand of Scopolamine Borate
ct-Arzneimittel Brand of Theophylline Sodium Glycinate
Progro TS
Sapoderm
Vetibenzamin
Lymphosarcoma
Bronchoparat
Jones Brand of Thrombin
Apiguard
Thymol Swarm Brand
Thrombocytopenias, Neonatal Alloimmune
CNTO 328 monoclonal antibody
Lymphoma, Diffuse
Diffuse Lymphomas
Lymphomas, Diffuse
Godecke Brand of Tilidine Hydrchloride Hemihydrate
Progro T-S
Venous Stasis Ulcers
Cavernous Hemangioma of Brain
Brain Cavernous Hemangioma
Alloimmune Thrombocytopenia, Neonatal
Neonatal Alloimmune Thrombocytopenias
Uniphyllin
Mundipharma Brand of Theophylline Sodium Glycinate
Triclosan Reckitt Brand
Ulcer, Venous Stasis
Agyria
Neonatal Alloimmune Thrombocytopenia
Embden-Meyerhof pathway, function
Aphthous ulceration
Job's syndrome
Tetanus immunoglobulin
Neonatal thrombocytopenia due to platelet alloimmunization
Fourth heart sound, S>4<, function
Aphthosis
Aphthous ulcer
Turban tumor
Glycopyrronium bromide
Factor IX complex agent
4-hydroxy-9-(2-hydroxy-3-((1-methylethyl)amino)propoxy)-7-methyl-5H-furo(3,2-g)(1)benzopyran-5-one
Benzenamine, 2,6-dichloro-4-((4,5-dihydro-1H-imidazol-2-yl)methyl)-, monohydrochloride
CDG IIg
CDG1C
CDGS2, FORMERLY
CLN4A
HSCR
CDG1L
C3 INACTIVATOR DEFICIENCY
GSD9B
HAMMAN-RICH DISEASE
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1
AGANGLIONIC MEGACOLON
TOOTH AGENESIS, SELECTIVE, 1
HYPODONTIA/OLIGODONTIA 1
CDG2G
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg
XPB/CS
CDGS5, FORMERLY
DYSPLASMINOGENEMIA
GOUT, PRPS-RELATED
Hypertonia later
HIRSCHSPRUNG DISEASE
BRANCHIOOTORENAL SYNDROME 1
BPAD
COMPLEMENT FACTOR I DEFICIENCY
CDG2E
PULMONARY DISEASE, CHRONIC OBSTRUCTIVE
OSTEOPETROSIS, AUTOSOMAL DOMINANT, TYPE II
BALDNESS, MALE PATTERN
STHAG1
Increased serum ketones
DVA
GSD IXb
COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY
Cerebral cavernous malformations
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE I, WITH DEFICIENT GLYCOSYLATION OF DOLICHOL-LINKED OLIGOSACCHARIDE, FORMERLY
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE V, FORMERLY
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE II, FORMERLY
CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE
OSTEOPETROSIS, AUTOSOMAL DOMINANT 2
BOR1
CDGIIg
Abnormal isoelectric focusing of serum transferrin, type I pattern
Duplicate ureter
CDG2A
HYPER-IgE SYNDROME, AUTOSOMAL DOMINANT
HIES, AUTOSOMAL DOMINANT
HYPERCHYLOMICRONEMIA WITH HYPERPREBETALIPOPROTEINEMIA, FAMILIAL
Methyldopa anhydrous
Pinocchio syndrome
Congenital anomaly of anterior segment of eye
BIBW-2992
MGCD-0103
BIBW2992
MGCD0103
MGCD 0103
eslicarbazepine acetate
Calamine lotion, phenolated
tetrazolast meglumine
Failure to thrive in infant
Finding of ECG U wave
Pathologic calcification, calcified structure
chromic chloride hexahydrate
Alphacetylmethadol
ALPHACETYLMETHADOL
CT-011
Congenital Pure Red Cell Aplasia
Docosahexaenoic Acid
VENTRICULAR HYPERTROPHY
Patupilone
Hashimoto's Thyroiditis
HEXAMINOLEVULINATE HYDROCHLORIDE
LOBENZARIT SODIUM
Manganese Chloride Tetrahydrate
PEG-SN38
S-Allyl Cysteine
2,7,8-trimethyl-2-(4,8,12-trimethyltridecyl)chroman-6-ol
Acedoben
[18F]FACBC
YN968D1
Aurora A Kinase Inhibitor MLN8237
CHK1 Inhibitor PF-477736
ACUTE INFERIOR WALL MI
Acute Posterior Wall Myocardial Infarction
ANTERIOR WALL MYOCARDIAL INFARCTION
GLISENTIDE
MANGANESE CHLORIDE TETRAHYDRATE
Vitamin A
L-5-Hydroxytryptophan
ENOFELAST
Gemcabene
GEMCABENE
Glisentide
Greig's Syndrome
Elevated Core Body Temperature
SULFAMETOMIDINE
Trigeminy
HA22
Immunotoxin CAT-8015
Geroquinol
Insulin Aspart
Lobenzarit Sodium
MISTLETOE EXTRACT
Nicotinamide
NON Q WAVE MYOCARDIAL INFARCTION
Selective Androgen Receptor Modulator MDV3100
Sulfametomidine
TOMOGLUMIDE
3-[2-[7a-methyl-1-(1,4,5-trimethylhex-2-enyl)-1,2,3,3a,5,6,7,7a-octahydroinden-4-ylidene]ethylidene]-4-methylidene-cyclohexan-1-ol
ACEDOBEN
ETHYL ICOSAPENTATE
GEROQUINOL
Greig Syndrome
Hashimoto Thyroiditis
Hexaminolevulinate Hydrochloride
Anti-CCR4 Monoclonal Antibody KW-0761
Secretin Human
SECRETIN HUMAN
SINUS ARREST/PAUSE
SCH-D
Vitamin D
Levothym
Acitazanolast
Benzoylpas
BENZOYLPAS
AEZS-108
DOXO-EMCH
Acute Inferior Wall Myocardial Infarction
Acute Lateral Wall Myocardial Infarction
Anterior Wall Myocardial Infarction
Ventricular Hypertrophy
Enofelast
Idiopathic Thrombocytopenia Purpura
Idiopathic Thrombocytopenia
Phospholipid with Choline
Vitamin B-3
Sinus arrest/pause
Tomoglumide
Alum, Potassium
KM87O
Premature atrial complexes
Bromofenofos
Insulin Aspart Recombinant
Non Q Wave Myocardial Infarction
Polyethyleneglycol-7-ethyl-10-hydroxycamptothecin
TRIGEMINY
Vofopitant
VOFOPITANT
ACITAZANOLAST
Benaxibine
BENAXIBINE
Cancer Disease Progression
Doxorubicin-EMCH
ACUTE LATERAL WALL MI
ACUTE POSTERIOR WALL MI
Ethyl Icosapentate
5-Formyltetrahydrofolate
Mifamurtide
Nicotinic Acid Amide
NKTR 102
Separation Anxiety Disorder
Anxiety Disorder, Separation
Familial Reticuloendothelioses
Omenns Syndrome
SEPARATION ANXIETY DIS
Reticuloendothelioses, Familial
Teratomas, Benign
Multisynostotic Osteodysgenesis
Adherence, Medication
sodium thiosulfate anhydrous
Syndrome, Omenn
Familial Reticuloendotheliosis
Omenn's Syndrome
Syndrome, Omenn's
Antley-Bixler Syndrome, Autosomal Dominant
Teratoma, Benign
Teratoma, Cystic
Antley Bixler Syndrome, Autosomal Dominant
Osteodysgenesis, Multisynostotic
Medication Adherence
Benign Teratoma
Benign Teratomas
Chromosome 6-Linked Autosomal Recessive Parkinsonism
Acute Autoimmune Neuropathies
Autoimmune Neuropathies, Acute
Autoimmune Neuropathy, Acute
Neuropathies, Acute Autoimmune
Neuropathy, Acute Autoimmune
Acute Inflammatory Polyneuropathies
Inflammatory Polyneuropathies, Acute
Polyneuropathies, Acute Inflammatory
Inflammatory Polyneuropathy, Acute
Acute Inflammatory Polyradiculoneuropathies
Inflammatory Polyradiculoneuropathies, Acute
Polyradiculoneuropathies, Acute Inflammatory
Ag3340
Articulatory Apraxia
Apraxias, Articulatory
Articulatory Apraxias
Type II Arnold-Chiari Malformation
Articulatory Dyspraxia
Dyspraxia, Articulatory
Articulatory Dyspraxias
Dyspraxias, Articulatory
Cancer, Therapy-Associated
Cancers, Therapy-Associated
Therapy Associated Cancer
Therapy-Associated Cancers
Cancer, Treatment-Associated
Cancers, Treatment-Associated
Treatment Associated Cancer
Treatment-Associated Cancer
Treatment-Associated Cancers
Familial Parkinson Disease, Autosomal Recessive
Parkinson Disease, Familial, Autosomal Recessive
Juvenile Parkinson Disease, Autosomal Recessive
Juvenile Parkinsonism, Autosomal Recessive
Parkinsonism, Juvenile, Autosomal Recessive
Autosomal Recesssive Juvenile Parkinsonism
Babinski Sign Positive
Babinski's Reflex
Reflex, Babinski's
Babinski Sign
Babinski's Sign
Landry Guillain Barre Syndrome
Syndrome, Landry-Guillain-Barre
Guillaine Barre Syndrome
Syndrome, Guillaine-Barre
Congenital afibrinogenemia
Bilateral Deafness
Deafness, Bilateral
Complete Blindness
Brain Hemorrhage, Cerebral
Brain Hemorrhages, Cerebral
Cerebral Brain Hemorrhage
Cerebral Brain Hemorrhages
Hemorrhage, Cerebral Brain
Hemorrhages, Cerebral Brain
Cacosmias
Cancers, Cervix
Cancer, Therapy-Related
Cancers, Therapy-Related
Therapy Related Cancer
Therapy-Related Cancer
Therapy-Related Cancers
Cancer, Treatment-Related
Cancers, Treatment-Related
Treatment Related Cancer
Treatment-Related Cancer
Treatment-Related Cancers
Cerebral Parenchymal Hemorrhage
Cerebral Parenchymal Hemorrhages
Hemorrhage, Cerebral Parenchymal
Hemorrhages, Cerebral Parenchymal
Parenchymal Hemorrhage, Cerebral
Parenchymal Hemorrhages, Cerebral
Cerebrum Hemorrhage
Cerebrum Hemorrhages
Hemorrhage, Cerebrum
Hemorrhages, Cerebrum
Fourth Cranial Nerve Diseases
Cranial Nerve IV Diseases
Dandy Walker Syndrome, Familial
Dandy-Walker Syndrome, Familial
Familial Dandy-Walker Syndrome
Syndrome, Familial Dandy-Walker
Deficiency Disease, Galactokinase
Galactokinase Deficiency Diseases
Trochlear Nerve Disease
Trochlear Nerve Diseases
Trochlear Nerve Disorder
Trochlear Nerve Disorders
Dyslalias
Dysosmias
Encephalitis, Russian Spring Summer
Russian Spring Summer Encephalitis
Russian Spring-Summer Encephalitis
Spring-Summer Encephalitis, Russian
Encephalopathies, Hypoxic-Ischemic
Encephalopathies, Ischemic-Hypoxic
Encephalopathy, Hypoxic Ischemic
Encephalopathy, Hypoxic-Ischemic
Hypoxic Ischemic Encephalopathy
Hypoxic-Ischemic Encephalopathies
Ischemic Hypoxic Encephalopathy
Ischemic-Hypoxic Encephalopathy
Great Toe Paradoxical Extensor Reflex
Paradoxical Extensor Reflex, Great Toe
Extensor Plantar Reflex
Plantar Reflex, Extensor
Reflex, Extensor Plantar
Extensor Plantar Response
Extensor Plantar Responses
Plantar Response, Extensor
Plantar Responses, Extensor
Response, Extensor Plantar
Responses, Extensor Plantar
CUV1647
Hemorrhage, Intracerebral
Hemorrhages, Intracerebral
Intracerebral Hemorrhages
Hyperactivity, Psychomotor
Psychomotor Hyperactivity
Hypermetrias
lutex
Meningioma, Papillary
Meningiomas, Papillary
Papillary Meningiomas
Neoplasm, Thymic
Neoplasms, Thymic
Thymic Neoplasm
Thymic Neoplasms
Neuropathies, Trochlear
Neuropathy, Trochlear
Trochlear Neuropathies
Trochlear Neuropathy
Nystagmus, Rotational
Psychomotor Restlessness
Restlessness, Psychomotor
DBA6
PHP1C
INFANTILE POLYARTERITIS
Hypothyroidism, secondary
Type II Arnold Chiari malformation
EIEE1
INFANTILE SPASM SYNDROME, X-LINKED 1
EBV INFECTION, SEVERE, SUSCEPTIBILITY TO
TELECANTHUS-HYPOSPADIAS SYNDROME
THYROTROPIN DEFICIENCY, ISOLATED
Hearing deficit
CIO
GASTRIC CANCER, FAMILIAL DIFFUSE
HED
HYPERTROPHY OF THE BREAST, JUVENILE
AGA1
DIAMOND-BLACKFAN ANEMIA 6
PHP IC
LQT2/9
ARB
BDMR
DFNX3
OPITZ GBBB SYNDROME, TYPE I
HYPERTELORISM WITH ESOPHAGEAL ABNORMALITY AND HYPOSPADIAS
PKU
MMM
JALILI SYNDROME
PARK
MOLAR I REINCLUSION
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 2
MODY, TYPE 2
ALOPECIA, ANDROGENETIC, 1
PSEUDOHYPOPARATHYROIDISM, TYPE IA
BFIC1
FAMILIAL IDIOPATHIC OSTEOARTHROPATHY OF CHILDHOOD
Congenital absence of nails (anonychia)
OSTEOPOROSIS
OSTEOARTHRITIS SUSCEPTIBILITY 2
ANTIPHOSPHOLIPID SYNDROME, FAMILIAL
ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE
ACROMEGALY DUE TO PITUITARY ADENOMA
Flexion contractures (PIP joints)
JUVENILE POLYPOSIS, INFANTILE
LONG QT SYNDROME 2/9
Prenatal growth failure
ISSX1
XMESID
Periventricular heterotopia
High-bridged nose
CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 1
Photogenic epilepsy
Hepatocyte necrosis
Wilms tumor, increased risk of
EPIDERMOLYSIS BULLOSA, GENERALIZED ATROPHIC BENIGN
PHP2
Multiminicore myopathy
IMMUNE THROMBOCYTOPENIC PURPURA
ODONTOCHONDRODYSPLASIA
OS1
NEVUS, KERATINOCYTIC, NONEPIDERMOLYTIC
HOA
MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 1
JHB
FIS
ISOLATED FAMILIAL SOMATOTROPINOMA
IFS
NEUROEPITHELIOMA, PERIPHERAL
PNE
Thickened clavicles
LEUKOENCEPHALOPATHY WITH AXENFELD-RIEGER ANOMALY
DEAFNESS, X-LINKED 3
OPITZ GBBB SYNDROME, X-LINKED
GGGB1
HYPERTELORISM-HYPOSPADIAS SYNDROME
CURRARINO IDIOPATHIC OSTEOARTHROPATHY
Decreased platelet aggregation
ODCD
ANCELL-SPIEGLER CYLINDROMAS
EBDCT
GIGANTOMASTIA, JUVENILE
PHP1A
PITUITARY ADENOMA, GROWTH HORMONE-SECRETING
JUVENILE POLYPOSIS OF INFANCY
Abdominal wall laxity
DEAFNESS, AUTOSOMAL DOMINANT 22
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1
OPITZ SYNDROME
REGIONAL ENTERITIS
Smooth tongue
Pharyngeal cancer
AXENFELD-RIEGER SYNDROME, TYPE 1
NEVUS, EPIDERMAL
OS2
PSEUDOHYPOPARATHYROIDISM, TYPE IC
FURLONG SYNDROME
INFECTIOUS MONONUCLEOSIS, SEVERE, SUSCEPTIBILITY TO
Varicella zoster infection
Oligodendroglioma
Elevated parathyroid hormone
Esophageal lesions
Onset at birth or infancy
Chronic renal disease
LEBER CONGENITAL AMAUROSIS 1
MS1
PHP IA
SOMATOTROPINOMA, FAMILIAL ISOLATED
OSTEOPOROSIS, SUSCEPTIBILITY TO
INFANTILE EPILEPTIC-DYSKINETIC ENCEPHALOPATHY
Asymmetric face
MYELOFIBROSIS WITH MYELOID METAPLASIA
LUTEINIZING HORMONE RESISTANCE, FEMALE
DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, AND MENTAL RETARDATION SYNDROME
CONE-ROD DYSTROPHY AND AMELOGENESIS IMPERFECTA
Recurrent aphthous stomatitis
AITP
RIEGER SYNDROME, TYPE 1
BMND
OSTEOARTHRITIS SUSCEPTIBILITY 1
NEVI FLAMMEI, FAMILIAL MULTIPLE
SOMATOTROPHINOMA, FAMILIAL
Aluminum Sulfate Anhydrous
S-(N-(3-Aminopropyl)-2-aminoethyl)thiophosphoric Acid Trihydrate
Sangostasin
Betavel
GCPS
Growth-hormone-releasing Factor Analog
Vestibular Disorder
Lucatumumab
Glutamyltryptophan
Phantom Pain
Poliovirus Antigen, B
Rotavirus G1 P(8) Live Antigen, A
R788 Sodium
Streptococcus pneumoniae Type 19A Polysaccharide Antigen, A
STREPTOCOCCUS PNEUMONIAE TYPE 1 POLYSACCHARIDE ANTIGEN, A
STREPTOCOCCUS PNEUMONIAE TYPE 20 POLYSACCHARIDE ANTIGEN, A
STREPTOCOCCUS PNEUMONIAE TYPE 7F POLYSACCHARIDE ANTIGEN, A
STREPTOCOCCUS PNEUMONIAE TYPE 8 POLYSACCHARIDE ANTIGEN, A
TECALCET HYDROCHLORIDE
S-2-(3-Aminopropylamino)ethylphosphorothioic Acid Trihydrate
Dimevamida
AV-299
BANOXANTRONE
Chronic Renal Disease
Enadel
Triiron Tetraoxide
GOLOTIMOD
Greig Cephalosyndactyly Syndrome
Growth Hormone-Releasing Hormone Analogue
GHRF Analog
Lithium Cation
Lymphoplasmacytic Lymphoma
(131)I-MIBG
Mozavaptan
Neisseria meningitidis Group C Polysaccharide Antigen, A
Neisseria meningitidis Group W-135 Polysaccharide Antigen, A
Prostate-Secretory Protein-94-Derived Peptide PCK3145
PIMAVANSERIN
Progesterone Receptor Antagonist ZK 230211
RAW SUGAR
Feeling of Restlessness
RPLE
Split-Hand/Foot Malformation Type 1
STREPTOCOCCUS PNEUMONIAE TYPE 22F POLYSACCHARIDE ANTIGEN, A
STREPTOCOCCUS PNEUMONIAE TYPE 2 POLYSACCHARIDE ANTIGEN, A
Streptococcus pneumoniae Type 33F Polysaccharide Antigen, A
Streptococcus pneumoniae Type 9N Polysaccharide Antigen, A
Somatropin
Recombinant GH
3-Pyridinecarboxamide, N-(2,3-dihydro-3,3-dimethyl-1H-indol-6-yl)-2-((4-pyridinylmethyl)amino)-, phosphate (1:2)
2-[(3-Aminopropyl)amino]ethanethiol Dihydrogen Phosphate Ester Trihydrate
Banoxantrone
BENMOXIN
BUTETHAMINE HYDROCHLORIDE
Durezol
EGG PHOSPHOLIPIDS
ETHER
Black Iron Oxide
Glycyrrhiza glabra Root
Macrogol 3350-Based Iso-Osmotic Oral Laxative
IDEC-2B8
Paraffin Oil
Poliovirus Type 1 Inactivated Antigen, A
SDZ 212-713
ENA 713 Free Base
Streptococcus pneumoniae Type 11A Polysaccharide Antigen, A
STREPTOCOCCUS PNEUMONIAE TYPE 14 POLYSACCHARIDE ANTIGEN, A
Streptococcus pneumoniae Type 17F Polysaccharide Antigen, A
STREPTOCOCCUS PNEUMONIAE TYPE 3 POLYSACCHARIDE ANTIGEN, A
STREPTOCOCCUS PNEUMONIAE TYPE 5 POLYSACCHARIDE ANTIGEN, A
TIVIRAPINE
Monoclonal Antibody Anti-Avb3 Integrin Medi-522
Adipiplon
ADIPIPLON
ANGOSTURA BARK
9,10-Anthracenedione, 1,4-bis((2-(dimethylamino)ethyl)amino)-5,8-dihydroxy-, N,N'-dioxide
Benfurodil Hemisuccinate
Prostin 15M
4-(5,6,7,8-Tetrahydroimidazo(1,5-a)pyridin-5-yl)benzonitrile
Magnetic Black
Macrogol 3350-Based Iso-Osmotic Laxative
GHRH Analogue
GRF Analog
Phosphoinositide-3 Kinase Delta Inhibitor CAL-101
Pneumocystis Jiroveci Pneumonia
Pneumocystis
Rieger Syndrome Type 1
M-((S)-1-(Dimethylamino)ethyl)phenyl Ethylmethylcarbamate
ROTAVIRUS G1 P(8) LIVE ANTIGEN, A
Tegafur, mixture with Gimeracil and Potassium Oxonate
STREPTOCOCCUS PNEUMONIAE TYPE 23F POLYSACCHARIDE ANTIGEN, A
Streptococcus pneumoniae Type 4 Polysaccharide Antigen, A
TECADENOSON
Tecalcet Hydrochloride
Tivirapine
ULMW heparin AVE5026
(+-)-alpha-Tocopherol
Megimide
Benmoxin
Chronic Kidney Disease
CYCLOPENTAMINE HYDROCHLORIDE
Iron Black
Hypothermia
Li+
LITHIUM CATION
Heavy Mineral Oil
PHENOTHIAZINE
Pimavanserin
Piperazine, Hydrochloride (1:2)
Poliovirus Type 2 Inactivated Antigen, A
Restless
SAPROPTERIN
STREPTOCOCCUS PNEUMONIAE TYPE 10A POLYSACCHARIDE ANTIGEN, A
Streptococcus pneumoniae Type 12F Polysaccharide Antigen, A
Streptococcus pneumoniae Type 9V Polysaccharide Antigen, A
Thrombin Alfa
OCX-191
IVth Cranial Nerve Disorder
Adrenal Cortical Insufficiency
Alu-Tab
ATRELEUTON
Butethamine Hydrochloride
Fosbretabulin Disodium
Phenol, 2-methoxy-5-[(1Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]-, Dihydrogen Phosphate, Disodium Salt
PELITINIB
Gd-DOTA
GLYCERYL PALMITATE
IDEC-129
Implant Infection
MOZAVAPTAN
XL880
PCP
PJP
STREPTOCOCCUS PNEUMONIAE TYPE 15B POLYSACCHARIDE ANTIGEN, A
Streptococcus pneumoniae Type 19F Polysaccharide Antigen, A
Growth Hormone, Human
THROMBIN ALFA
Human Thrombin (Recombinant, Glycosylated)
Thrombin (Synthetic Human)
Ureteral Stricture
PRALATREXATE
(+/-)-alpha-Tocopherol
BR-222
5-Ethyl-5-(1-methylpropyl)barbituric Acid
Pelitinib
Primovist
Gastrointestinal System Stenosis
Glyceryl Palmitate
Somatocrinin Analogue
Sinestrol
5-(o-(2-(Dimethylamino)ethoxy)phenyl)-3-phenyl-1,2,4-oxadiazole
Lithium Ion
Noctan
Neisseria meningitidis Group Y Polysaccharide Antigen, A
Glu-trp
Pneumocystis Pneumonia
Poliovirus Type 3 Inactivated Antigen, A
Pustular Lesion
Raw Sugar
huS2C6
Tecadenoson
TESMILIFENE HYDROCHLORIDE
Ulcerated
Ulcerating
Watering Eyes
Cholinesterase Inhibitor
(+-)-(2S)-2-((4,6-Dimethylpyrimidin-2-yl)oxy)-3-methoxy-3,3-diphenylpropanoic Acid
Aminopropylaminoethylthiophosphoric Acid Trihydrate
Aminophylline Dihydrate
Angostura Bark
BENFURODIL HEMISUCCINATE
Tolestan
Cyclopentamine Hydrochloride
Egg Phospholipid
Behenic Monoglyceride
Macrogol 3350/Electrolytes Oral Laxative
Golotimod
Growth Hormone Secretagogue
Dimerin
Heavy Liquid Petrolatum
Piperazine Hydrochloride
Pneumocystis Carinii Pneumonia
Poliovirus Antigen, A
Retinoid 9cUAB30
Rimoprogin
RIMOPROGIN
Sapropterin
Splenic Lymphoplasmacytic Lymphoma
Split-Hand/Foot Malformation 1
NGX 424
Yellow Fever Virus Live Antigen, A
YELLOW FEVER VIRUS LIVE ANTIGEN, A
Confusional arousal disorder
5 Formyltetrahydropteroylglutamate
Maculopathy, Age-Related
Deficiency, Uroporphyrinogen Synthase
Synthase Deficiency, Uroporphyrinogen
Primary Toni Debre Fanconi Syndrome
Macular Dystrophies
Maculopathies, Age Related
Age-Related Macular Degeneration
AGE RELAT MACULOPATHY
Age Related Maculopathies
Deficiency, Hydroxymethylbilane Synthase
Idiopathic De Toni-Debre-Fanconi Syndrome
Neonatal De Toni-Debre-Fanconi Syndrome
Neonatal De Toni Debre Fanconi Syndrome
AGE RELAT MACULOPATHIES
MACULOPATHY AGE RELAT
Macular Degeneration, Age-Related
Macular Degenerations, Age-Related
Hydroxymethylbilane Synthase Deficiency
Hydroxymethylbilane Synthase Deficiencies
Synthase Deficiency, Hydroxymethylbilane
Synthase Deficiencies, Uroporphyrinogen
Age Related Macular Degeneration
Age-Related Macular Degenerations
Degeneration, Age-Related Macular
Degenerations, Age-Related Macular
Age-Related Maculopathy
Toni-Debre-Fanconi Syndrome, Primary
Macular Dystrophy
Dystrophies, Macular
Disabilities, Intellectual
Deficiencies, Hydroxymethylbilane Synthase
Synthase Deficiencies, Hydroxymethylbilane
Deficiencies, Uroporphyrinogen Synthase
Uroporphyrinogen Synthase Deficiencies
Acute, Inflammatory Polyneuropathy
Polyneuropathy Acute, Inflammatory
Acute Inflammatory Demyelinating Polyneuropathy
veltuzumab
Arnold-Chiari Malformation, Type 2
Arnold Chiari Malformation, Type 2
Idiopathic De Toni Debre Fanconi Syndrome
Primary Toni-Debre-Fanconi Syndrome
Maculopathy, Age Related
MACULOPATHIES AGE RELAT
Intellectual Disabilities
Uroporphyrinogen Synthase Deficiency
Toni-Debre-Fanconi Syndrome
Toni Debre Fanconi Syndrome
Age-Related Maculopathies
Dystrophy, Macular
Maculopathies, Age-Related
Age Related Maculopathy
Inflammatory Polyneuropathy Acutes
Job syndrome
Bietti crystalline retinopathy
Dupuytren disease
spironolactone, althiazide drug combination
hydrocortisone, oxytetracycline drug combination
pseudoephedrine, triprolidine drug combination
estradiol, estriol drug combination
Pregn-4-ene-21-carboxylic acid, 7-(acetylthio)-17-hydroxy-3-oxo-, gamma-lactone, (7alpha,17alpha)-, mixt. with 6-chloro-3,4-dihydro-3-((2-propenylthio)methyl)-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide
aspirin, meprobamate drug combination
Linagliptin
acetaminophen, butalbital, caffeine drug combination
sulfamethizole, sulfaethidole drug combination
Benzoic acid, 2-(acetyloxy)-, mixt. with (S-(R*,S*))-3-(dimethylamino)-2-methyl-1-phenyl-1-(phenylmethyl)propyl propanoate 2-naphthalenesulfonate
AEB071
harnosal
aspirin, dextropropoxyphene drug combination
acetaminophen, caffeine, paracetamol drug combination
triprolidine, pseudoephedrine drug combination
isoniazid, pyrazinamide, rifampin drug combination
aspirin, caffeine, codeine drug combination
aspirin - dextropropoxyphene
indapamide, perindopril drug combination
sulfaethidole, sulfamethizole drug combination
ATD3
Pulmonary arterial hypertension
PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL
FNEPPK
GSD11
3M1
SITUS INVERSUS VISCERUM
VERTIGO, BENIGN RECURRENT
FTDMND
FOCAL NONEPIDERMOLYTIC PALMOPLANTAR KERATODERMA
NASOPHARYNGEAL CANCER
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT
TETRAAMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES
Thickening of the helices
Motor dysfunction
Epidermal hyperplasia
Prematurity
KFSDX
THREE M SYNDROME 1
GLYCOGEN STORAGE DISEASE IXb
PHOSPHORYLASE KINASE DEFICIENCY OF LIVER AND MUSCLE, AUTOSOMAL RECESSIVE
PRIMARY OVARIAN INSUFFICIENCY, FRAGILE X-ASSOCIATED
HETEROTAXY, VISCERAL, 5, AUTOSOMAL
FRONTOFACIONASAL DYSPLASIA
FFND
DIHYDROPYRIMIDINURIA
PULMONARY ARTERIAL HYPERTENSION
Neutrophilia
Thickened corpus callosum
MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED
FRONTOFACIONASAL DYSOSTOSIS
HYPOKALEMIC PERIODIC PARALYSIS
ALSFTD
KERATODERMA, FOCAL NONEPIDERMOLYTIC PALMOPLANTAR
GSD XI
NASOPHARYNGEAL CARCINOMA
BIFID NOSE, AUTOSOMAL RECESSIVE
BRV
PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA
RCC
Normal cognition
CMT2I
NPCA
TETRAAMELIA, AUTOSOMAL RECESSIVE
SIV
CPHD5
PPH1 WITH HHT
HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1
HOKPP1
HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT
Ungual hypoplasia
LACTATE DEHYDROGENASE A DEFICIENCY
NPC
Gut malrotation
Hyperkinesia
PITUITARY HORMONE DEFICIENCY, COMBINED, 5
PULMONARY HYPERTENSION, PRIMARY, 1
PAH
Poor response to L-dopa treatment
2-methoxy-5-[(1Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]phenyl Disodium Phosphate
Atypical Chronic Myeloid Leukemia
HEMORRHAGE, CEREBRAL
VISION, LOSS OF
OSTEOLYSIS
SWOLLEN GLANDS
GLANDS, SWOLLEN
Multitargeted Tyrosine Kinase Inhibitor BIBF 1120
Fresolimumab
Urine Output Decreased
HUMAN RABIES VIRUS IMMUNE GLOBULIN
Obeticholic Acid
Triton X
FIBRINOGEN HUMAN
CARCAINIUM CHLORIDE
CLOFILIUM PHOSPHATE
Tofenacin Hydrochloride
TOFENACIN HYDROCHLORIDE
Tryptophan Hydroxylase Inhibitor LX1032
Trastuzumab-MCC-DM1 Immunoconjugate
Methylmethionine Sulfonium Chloride
Lad's Love Top
AV Mobitz I
Ambrosia bidentata Pollen
Ambrosia confertiflora Pollen
ATRIPLEX WRIGHTII POLLEN
Melilotus albus Pollen
Picea pungens Pollen
Pinus resinosa Pollen
Platanus hybrida Pollen
ROBINIA PSEUDOACACIA POLLEN
Rumex altissimus Pollen
SOLIDAGO CANADENSIS POLLEN
Xanthium strumarium var. canadense Pollen
Iodine I 123 Iodobenzamide
Resveratrol Formulation SRT501
TESTOSTERONE BUCYCLATE
Mecetronium
CAD
White blood cell decreased
Androgen Insensitivity Syndrome
GLUCOSE, LOW BLOOD
LOW BLOOD GLUCOSE
AESLIFE
Veltuzumab
HYPERTHERMIA
INSUFFICIENCY, VALVULAR
REGURGITATION, VALVULAR
FAILURE, RIGHT VENTRICULAR
STEALTH Liposomal Belotecan
Cannabis-Based Oromucosal Spray GW-1000-02
PARP Inhibitor AZD2281
Ringdex C
Phantom pain
Azoospermia
Platelet ADP Receptor Antagonist
LY 307640 Sodium
Human Rabies Virus Immune Globulin
Fibrinogen Human
Naepaine Hydrochloride
Acute Myeloid Leukemia with 11q23 Abnormalities
Trastuzumab-DM1
PRORENOATE
Excessive Blood Clotting
Atriplex polycarpa Pollen
BETULA ALLEGHANIENSIS POLLEN
Carya glabra Pollen
CHENOPODIUM BOTRYS POLLEN
Waardenburg Syndrome
JUNIPERUS PINCHOTII POLLEN
Phalaris arundinacea Pollen
Pinus rigida Pollen
Pinus sylvestris Pollen
QUERCUS LOBATA POLLEN
Quercus muehlenbergii Pollen
Quercus nigra Pollen
Lolium perenne ssp. multiflorum Pollen
PERRL
Peretinoin
Almorexant
APOLIZUMAB
BLOOD GLUCOSE, LOW
Lymphocyte count increased
AESDISAB
HYPOVENTILATION
LOSS OF VISION
VALVULAR INSUFFICIENCY
WEAKNESS
VENTRICULAR FAILURE, RIGHT
5-Aminolevulinic Acid Methyl Ester
Sodium Phosphate, Tribasic
Dexy Pearl Gamma-100
Watering eyes
Filaminast
Val-boro-Pro
Naluzotan
Human Rho(D) Immune Globulin
Ovine Digoxin Immune Fab
2-AMINOBUTYRIC ACID, DL
Carcainium Chloride
Von Willebrand Factor Human
Indacaterol
LIFICIGUAT
Amino Methacrylate Copolymer
Hypersensitivity Vasculitis
Southernwood Top
Carbonic Acid, Diammonium Salt
AV Mobitz II
Nonalcoholic Steatohepatitis
Beta-Mannosidosis
Centronuclear Myopathy
Acacia baileyana Pollen
Betula alleghaniensis Pollen
Betula papyrifera Pollen
CHENOPODIUM AMBROSIOIDES POLLEN
Citrus sinensis Pollen
EUPATORIUM CAPILLIFOLIUM POLLEN
Fraxinus latifolia Pollen
FRAXINUS LATIFOLIA POLLEN
QUERCUS PALUSTRIS POLLEN
Quercus virginiana Pollen
QUERCUS VIRGINIANA POLLEN
TILIA AMERICANA POLLEN
Typha latifolia Pollen
Lolium perenne var. Multiflorum Pollen
pan-PI3K/mTOR Inhibitor SF1126
LGA
Erythroblastosis Fetalis, Rh Disease
Tea Leaf
LEVOMETHADYL ACETATE
SAMARIUM SM-153 LEXIDRONAM PENTASODIUM
Lymphocytopenia
Lipoid Nephrosis
Minimal Change Disease
LUNG, OVERINFLATION OF
Hyaluronan
Acute Monoblastic and Monocytic Leukemia
Epicriptine
CKD - Chronic Kidney Disease
Orestin
NSTEMI
Thienopyridines
PRIFELONE
FILAMINAST
Lapine T-Lymphocyte Immune Globulin
2-Aminobutyric Acid, DL
Social History
VON WILLEBRAND FACTOR HUMAN
Almurtide
Phenolate Sodium
Acute Myeloid Leukemia with t(9;11)(p22;q23); MLLT3-MLL
Acute Myeloid Leukemia with MLL Abnormalities
Melanotan I
Superparamagnetic Iron Oxide
Ibacitabine
1H-Purine-2,6-dione, 8-((3R)-3-amino-1-piperidinyl)-7-(2-butynyl)-3,7-dihydro-3-methyl-1-((4-methyl-2-quinazolinyl)methyl)-
Navuridine
3'H-Cyclopropa(6,7)Pregna-4,6-Diene-21-Carboxylic Acid, 6,7-Dihydro-17-Hydroxy-3-Oxo-, (6.Alpha.,7.Alpha.,17.Alpha.)-
Sodium Thiosulfate Anhydrous
Sodium Thiosulfate, Anhydrous
NASH - Nonalcoholic Steatohepatitis
Cerebral Cavernous Malformation
Myotonic Dystrophy
AMBROSIA CONFERTIFLORA POLLEN
Artemisia ludoviciana Pollen
Atriplex wrightii Pollen
Carpinus caroliniana Pollen
MELILOTUS ALBUS POLLEN
MELILOTUS OFFICINALIS POLLEN
Morella cerifera Pollen
Pinus nigra Pollen
Pinus thunbergii Pollen
Poa annua Pollen
Quercus garryana Pollen
Ulmus crassifolia Pollen
ULMUS CRASSIFOLIA POLLEN
ULMUS PARVIFOLIA POLLEN
Large for Gestational Age
TEA LEAF
Enzacamene
Appendix Cancer
9-Nitro-20(S)-camptothecin
Tegafur-gimeracil-oteracil Potassium
FOSBRETABULIN DISODIUM
Atypical Chronic Myeloid Leukemia, BCR-ABL1 Negative
131I-Chlorotoxin
Therapy-Related Malignant Neoplasm
OVERINFLATION OF LUNG
VALVULAR REGURGITATION
FIGITUMUMAB
SKF 385
Anti-CD20 Monoclonal Antibody R7159
Acute Monoblastic Leukemia and Acute Monocytic Leukemia
1-(2-Deoxy-beta-L-erythropentafuranosyl)-5-methyl-2,4(1H)-pyrimidinone
Anhydrous Dibasic Calcium Phosphate
Thienopyridine Antiplatelet Agent
WR 4629
Human Cytomegalovirus Immune Globulin
HUMAN HEPATITIS B VIRUS IMMUNE GLOBULIN
LAPINE T-LYMPHOCYTE IMMUNE GLOBULIN
Capmul MCM
Diammonium Carbonate
Fosfonet Sodium Anhydrous
AV MOBITZ II
NAVURIDINE
6,7-Dihydro-17-Hydroxy-3-Oxo-3'H-Cyclopropa(6,7)-17.Alpha.-Pregna-4,6-Diene-21-Carboxylate
Myotonia Congenita
AMBROSIA BIDENTATA POLLEN
Arrhenatherum elatius Pollen
ARRHENATHERUM ELATIUS POLLEN
Artemisia annua Pollen
ARTEMISIA ANNUA POLLEN
ARTEMISIA FRIGIDA POLLEN
CARPINUS CAROLINIANA POLLEN
Juniperus monosperma Pollen
Juniperus pinchotii Pollen
Maclura pomifera Pollen
Phleum pratense Pollen
Pinus contorta Pollen
QUERCUS MACROCARPA POLLEN
Robinia pseudoacacia Pollen
Rumex obtusifolius Pollen
Solidago canadensis Pollen
Tilia americana Pollen
Ulmus pumila Pollen
ULMUS PUMILA POLLEN
LOLIUM PERENNE SSP. MULTIFLORUM POLLEN
RhD Hemolytic Disease of the Newborn
PERETINOIN
ALMOREXANT
Carbamic Acid, N-[[4-[[(2-aminophenyl)amino]carbonyl]phenyl]methyl]-, 3- pyridinylmethyl Ester
Tri-O-acetyluridine
Vistonuridine
Coronary Artery Disease
Coronary Disease
Trichothiodystrophy Syndrome
BLEEDING, CEREBRAL
RIGHT VENTRICULAR FAILURE
Osteonecrosis of jaw
APO-066
AMG 888
TALABOSTAT MESYLATE
NALUZOTAN
ALMURTIDE
PHENOLATE SODIUM
METHYLMETHIONINE SULFONIUM CHLORIDE
DIAMMONIUM CARBONATE
Prorenoate
Dystrophia Myotonica 1
ARTEMISIA DRACUNCULUS POLLEN
Artemisia frigida Pollen
ARTEMISIA LUDOVICIANA POLLEN
ATRIPLEX POLYCARPA POLLEN
BACCHARIS HALIMIFOLIA POLLEN
BROUSSONETIA PAPYRIFERA POLLEN
CITRUS SINENSIS POLLEN
Eupatorium capillifolium Pollen
XYY Syndrome
Larix occidentalis Pollen
QUERCUS KELLOGGII POLLEN
Quercus macrocarpa Pollen
RUMEX OBTUSIFOLIUS POLLEN
TAXODIUM DISTICHUM POLLEN
Italian Ryegrass Pollen
Hydroxyprogesterone
Bolandiol Dipropionate
Dipenine
VITAMIN A
Detrusitol
PSVT
DEMENTIA
BLOOD LOSS
CEREBRAL HEMORRHAGE
VISION, IMPAIRED
IMPAIRED VISION
Hyaluronate
2-((R)-2-Methylpyrrolidin-2-yl)-1H-benzimidazole-4-carboxamide
Alum, Potassium, Dodecahydrate
Aluminum Potassium Sulfate (1:1:2) Dodecahydrate
Dimelin
CKD602 HCl
ANHYDROUS DIBASIC CALCIUM PHOSPHATE
5-Imino-13-deoxydoxoubicin
Talabostat Mesylate
((2R)-1-((2S)-2-amino-3-methylbutanoyl)pyrrolidin-2-yl)boronic Acid Methanesulfonate
Human Hepatitis B Virus Immune Globulin
NAEPAINE HYDROCHLORIDE
Clofilium Phosphate
Tofacine
Leukocytoclastic Vasculitis
Artemisia Procera Top
FERUMOXIDES NON-STOICHIOMETRIC MAGNETITE
Suprefact
ACACIA BAILEYANA POLLEN
Baccharis halimifolia Pollen
BETULA PAPYRIFERA POLLEN
Broussonetia papyrifera Pollen
Carya cordiformis Pollen
CARYA CORDIFORMIS POLLEN
CARYA GLABRA POLLEN
Chenopodium ambrosioides Pollen
XYY Karyotype
LARIX OCCIDENTALIS POLLEN
Leymus condensatus Pollen
Melilotus officinalis Pollen
Pinus palustris Pollen
Pinus taeda Pollen
QUERCUS GARRYANA POLLEN
Quercus kelloggii Pollen
Quercus lobata Pollen
QUERCUS MUEHLENBERGII POLLEN
QUERCUS NIGRA POLLEN
Autosomal Recessive Inherited Disorder
Pupils Equal Round and Reactive to Light Result
Hemolytic Disease of the Newborn
Rhesus D Hemolytic Disease of the Newborn
Rhesus Disease
ENZACAMENE
Levomethadyl Acetate
Vaginal hemorrhage
Testicular Feminization Syndrome
HYPOGLYCEMIA
LIFE THREATENING
Therapy Related Malignant Neoplasm
LOSS OF BLOOD
CEREBRAL BLEEDING
Anti-IGF-1R Recombinant Monoclonal Antibody MK-0646
Calcium Phosphate, Dibasic
Palladium-Bacteriochlorophyll Derivative WST11
Chronic kidney disease
Acute STEMI
Prifelone
FI 5978
HUMAN CYTOMEGALOVIRUS IMMUNE GLOBULIN
Pozanicline
POZANICLINE
INDACATEROL
Lificiguat
Acute Myeloid Leukemia with 11q23 (MLL) Abnormalities
S-Methymethionine Chloride
FOSFONET SODIUM ANHYDROUS
IBACITABINE
Ibafloxacin
IBAFLOXACIN
Istaroxime
ISTAROXIME
Merafloxacin
MERAFLOXACIN
Recombinant Human Anti-TGF-beta Monoclonal Antibody
Recombinant Human Anti-Transforming Growth Factor-beta Monoclonal Antibody
Necrotizing Enterocolitis
Artemisia dracunculus Pollen
Chenopodium botrys Pollen
JUNIPERUS MONOSPERMA POLLEN
LEYMUS CONDENSATUS POLLEN
MACLURA POMIFERA POLLEN
MORELLA CERIFERA POLLEN
Pinus elliottii Pollen
Pinus monticola Pollen
Quercus palustris Pollen
RUMEX ALTISSIMUS POLLEN
Taxodium distichum Pollen
TYPHA LATIFOLIA POLLEN
Ulmus parvifolia Pollen
Lolium multiflorum Pollen
Ear Dimple
RhD HDN
Testosterone Bucyclate
MECETRONIUM
BOLANDIOL DIPROPIONATE
DIPENINE
Fibrinogen in blood above reference range
Idiopathic retroperitoneal fibrosis
Elevated fibrinogen level
Ruspol
Pfizer Brand of Ergotamine Tartrate
G6PD Deficiency
Glucose-6-Phosphate Dehydrogenase Deficiencies
Primary Hyperthyroidism
Hyperimmunoglobulinemia E Syndromes
Hyperimmunoglobulin E, Recurrent Infection Syndrome
Ketoacidosis
Tardive Dyskinesia
Familial Atypical Mycobacterioses
amiloride, hydrochlorothiazide drug combination
calamine - phenol
Cataract, lamellar
Charcot-Marie-Tooth disease, Type 2I
Multiple cutaneous and uterine leiomyomatosis
Leiomyoma, multiple cutaneous
Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria
Carbohydrate-deficient glycoprotein syndrome, type 4
Meckel syndrome type 1
Ankyloblepharon filiforme adnatum cleft palate
Chromosome 18q syndrome
Late onset familial Alzheimer disease
Leber congenital amaurosis, type 9
Cylindromatosis, familial
Dermo-distortive urticaria
Cerebellar vermis aplasia
Apparent mineralocorticoid excess
Stickler syndrome, type 1
Familial chronic mucocutaneous candidiasis
Familial hypotransferrinemia
High density lipoprotein deficiency
Melanodermic leukodystrophy
Bronze Schilder disease
Rondec DM
Deficiency, G6PD
Dystonia, Tardive
Atypical Mycobacteriosis, Familial
Atypical Mycobacterioses, Familial
Mycobacteriosis, Familial Atypical
atropine sulfate - diphenoxylate hydrochloride
amiloride - hydrochlorothiazide
calamine lotion, phenolated
caffeine - sodium benzoate
Bellergal
acetaminophen - caffeine - paracetamol
Potassium and magnesium depletion
Swineherd's disease
Encephalopathy of childhood
Aicardi-Goutieres syndrome
Maple syrup urine disease, type 2
Gruber syndrome
Ehlers Danlos syndrome, Sack-Barabas type
Leber congenital amaurosis, type 5
Familial cylindromatosis
Congenital multiple arthrogryposis
X-linked adrenal hypoplasia congenita
Paroxysmal kinesigenic choreoathetosis
Cerebellar ataxia, early-onset, nonprogressive
Sialidoses, type 2
Torsion dystonia 1, autosomal dominant
PGA 1
Deletion 12p
RG7204
Synostosis, Metopic
G6PD Deficiencies
Innate Immune Response
Syndromes, Hyperimmunoglobulinemia E
Tardive Dystonia
atropine sulfate, diphenoxylate hydrochloride drug combination
calamine, phenol drug combination
Rice-field fever
L-2-hydroxyglutaric aciduria
47 XYY syndrome
Pentasomy X
Cystathioninuria
Leiomyoma, hereditary multiple, of skin
Multiple cutaneous and uterine leiomyomata 1
Pseudotoxoplasmosis syndrome
Psychogenic purpura
Iridogoniodysgenesis with somatic anomalies
Fibrosing mediastinitis
Congenital filiform fusion of the eyelids with cleft palate and/or cleft lip
Alzheimer disease type 2
Congenital adrenal hypoplasia
Tracheopathia osteoplastica
Cerebellar ataxia, congenital, nonprogressive, autosomal dominant
Aromatic L-amino acid decarboxylase deficiency
Ceroid lipofuscinosis, neuronal 8
Early onset torsion dystonia
APS 1
Monosomy 12p
Paralysis periodica paramyotonica
Deficiencies, Glucose-6-Phosphate Dehydrogenase
Deficiency, Glucose-6-Phosphate Dehydrogenase
Dehydrogenase Deficiencies, Glucose-6-Phosphate
Dehydrogenase Deficiency, Glucose-6-Phosphate
Ketoacidoses
Underbite
Dyskinesia, Tardive
Tardive Dystonias
Familial Atypical Mycobacteriosis
sulfadiazine - tetroxoprim
TLN 4601
TLN4601
Cane-cutter fever
YY syndrome
Chromosome X pentasomy
Cutaneous leiomyomata with uterine leiomyomata
Congenital disorder of glycosylation type 1D
D-Glycerate kinase deficiency
Congenital alopecia
Meckel syndrome type1
Usher syndrome, type 2A
Alzheimer disease associated with APOE E4
X-linked congenital adrenal hypoplasia
Pelvi-ureteric junction obstruction
Chromosome 12p deletion
Mesoectodermal dysplasia
Paramyotonia congenita of Von Eulenburg
Siemerling-Creutzfeldt disease
Immune Response, Innate
Immune Responses, Innate
Hyperimmunoglobulinemia E Syndrome
Syndrome, Hyperimmunoglobulinemia E
Underbites
Dystonias, Tardive
Dihydropyrimidinuria
caffeine benzoate
Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive
Acromesomelic dysplasia
Acromesomelic dwarfism Maroteux type
Rieger malformation
Ehlers Danlos syndrome type 4, autosomal dominant
Very long-chain acyl-CoA dehydrogenase deficiency
Glomerulopathy with fibronectin deposits
Fibronectin glomerulopathy
Kramer Syndrome
Adrenal aplasia
Heterotopia, Periventricular
morphine, naltrexone combination
RondecDM
Synostoses, Metopic
Deficiencies, G6PD
Primary Hyperthyroidisms
Dyskinesias, Tardive
sulfadiazine - trimethoprim
47, XYY syndrome
Perinuclear cataract
St Helena dysplasia
Rieger syndrome
Neutropenia, chronic familial
Erythrokeratodermia figurata, congenital familial, in plaques
Keratosis follicularis spinulosa decalvans cum ophiasi
Ehlers Danlos syndrome, ecchymotic type
Split-foot deformity with ectrodactyly and mandibulofacial dysostosis
VLCAD deficiency
Urogenital adysplasia, hereditary
18q syndrome
Amaurosis congenita of Leber, type 9
Adrenal hypoplasia congenita
Autoimmune polyendocrinopathy syndrome, type 1
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)
Hypoadrenocorticism with hypoparathyroidism and superficial moniliasis
Alliant Pharmaceuticals brand of chlorphenamine, dextromethorphan, phenylephrine drug combination
Metopic Synostosis
Metopic Synostoses
Innate Immune Responses
Tardive Oral Dyskinesias
Mycobacterioses, Familial Atypical
Atypical Mycobacteriosis, Familial Disseminated
caffeine, sodium benzoate drug combination
WAY VPA-985
Stuttgart disease
Cataract, zonular
Alopecia congenital
Osteogenesis imperfecta, type 2A
Vrolik type of osteogenesis imperfecta
Dysencephalia splachnocystica
Sclerosing mediastinitis
Ehlers Danlos syndrome, arterial type
Patterson Stevenson Fontaine syndrome
Autosomal dominant Vitreoretinochoroidopathy
Ankyloblepharon filiforme congenitum
Leber congenital amaurosis type 2
Jalili syndrome
Aplasia of cerebellar vermis
Cortisol 11-beta-ketoreductase deficiency
Aromatase deficiency
Stickler syndrome, vitreous type 1
Empty scrotum
Candidiasis familial chronic mucocutaneous, autosomal recessive
Dystonia musculorum deformans type 1
Atransferrinemia
Autoimmune polyendocrine syndrome, type 1
Restless legs syndrome 1
Glucose-6-Phosphate Dehydrogenase Deficiency
Glucose 6 Phosphate Dehydrogenase Deficiency
Nodular Sclerosing Hodgkin's Lymphoma
Hyperthyroidism, Primary
Tardive Dyskinesias
Tardive Oral Dyskinesia
Bellergal-S
TLN-4601
Chiari malformation type 2
Opalescent dentin
Mud fever
XYY syndrome
Epileptic encephalopathy, Lennox-Gastaut type
Reed's syndrome
Aicardi Goutieres syndrome
Axenfeld-Rieger syndrome
Congenital alopecia X-linked
Osteogenesis imperfecta congenita
Meckel Gruber syndrome
Erythrokeratodermia variabilis with erythema gyratum repens
Patterson Stevenson syndrome
Ankyloblepharon filiforme adnatum
Hereditary renal agenesis
Amaurosis congenita of Leber, type 2
Amaurosis congenita of Leber, type 5
Turban tumor syndrome
Glomerular nephritis, familial, with fibronectin deposits
Acromelalgia hereditary
Addison disease and cerebral sclerosis
Cylindroma of skin
Ancell-Spiegler cylindromas
muramyl tripeptide phosphatidylethanolamine
5-alpha reductase inhibitor
Hashimoto disease
chronic neutrophilic leukemia
2-Butenoic acid, 2-methyl-, (1aR,2S,5R,5aS,6S,8aS,9R,10aR)-1a,2,5,5a,6,9,10,10a- octahydro-5,5a-dihydroxy-4-(hydroxymethyl)-1,1,7,9-tetramethyl-11-oxo-1H-2,8a- methanocyclopenta[a]cyclopropa[e]cyclodecen-6-yl ester, (2Z)-
Kostmann syndrome
CHIR-265
Cyclodextrin-Based Polymer-Camptothecin CRLX101
Anti-CD22 Immunotoxin CAT-8015
Poliovirus Type 2 Inactivated Antigen, B
TRASTUZUMAB EMTANSINE
PINUS TAEDA POLLEN
POA ANNUA POLLEN
Pupils Equal, Round and Reactive to Light
4-Methylbenzylidene Camphor
Levacetylmethadol
LAAM
Triethyl(2-Hydroxyethyl)Ammonium Dicyclopentylacetate
SURINABANT
Piperidione
Dihyprylone
Histidine Hydrochloride
Activin Receptor-like Kinase 1 Inhibitor ACE-041
Congenital Musculoskeletal Defect
Opaviraline
Lexidronam
CHENODEOXYCHOLIC ACID, SODIUM SALT
LNA-RNA Antagonist EZN-3042
Fetal Heart Rate Acceleration
Benzyl Violet
Food Violet 2
Vaginal Bleeding
second cancer
Phosphatidylinositol 3-kinase Inhibitor ZSTK474
visilizumab
renal failure
Kostmann neutropenia
tyrosine kinase inhibitor BIBF 1120
Cinnamomum Aromaticum Bark Oil
False Cinnamon Oil
Dalfampridine
PA-457 di-NMG
POLIOVIRUS TYPE 3 ANTIGEN (FORMALDEHYDE INACTIVATED)
Trastuzumab Emtansine
Onaclostox
Anti-NGF Monoclonal Antibody JNJ-42160443
PHALARIS ARUNDINACEA POLLEN
PINUS CONTORTA POLLEN
PINUS NIGRA POLLEN
PINUS RESINOSA POLLEN
1-Hexadecanaminium, N-Ethyl-N,N-Dimethyl
Acetyl-L-Carnitine
Benzeneethanol, .Beta.-(2-(Dimethylamino)Propyl)-.Alpha.-Ethyl-.Beta.-Phenyl-, Acetate (Ester), (-)-
Nebidrazine
PIPERIDIONE
PHENYLBUTYRIC ACID
ACE-041
Alpha-Methyl-N-(2,2,2-Trichloroethylidene)Phenethylamine
AW-10
WA 184
IMC-20D7S
Diphtheria Toxoid/Tetanus Toxoid/Acellular Pertussis Vaccine Adsorbed
Hormone Imbalance
Benzenemethanaminium, N-(4-((4-(dimethylamino)phenyl)(4-(ethyl((3-sulfophenyl)methyl)amino)phenyl)methylene)-2,5-cyclohexadien-1-ylidene)-N-ethyl-3-sulfo-, Inner Salt, Sodium Salt
R788 Free Acid
Talastine Hydrochloride
Hemoglobin H Disease
BROVANEXINE HYDROCHLORIDE
Lysine Monohydrate
ovarian borderline malignant tumor
dementia
Sinoatrial Node Exit Block
congenital hypoplastic anemia
anti-CD22 immunotoxin CAT-8015
PARP-1 inhibitor AG014699
Oncaspar-IV
PICEA PUNGENS POLLEN
Bicyclo(2.2.1)Heptan-2-One, 1,7,7-Trimethyl-3-((4-Methylphenyl)Methylene)-
5,6-Dihydro-9,10-Dimethoxybenzo(G)-1,3-Benzodioxolo(5,6-A)Quinolizinium Chloride
Berberine Chloride Dihydrate
(-)-6-(Dimethylamino)-4,4-Diphenyl-3-Heptanol Acetate (Ester)
(2R)-2-((1S)-6,7-Dimethoxy-1-(2-(4-(Trifluoromethyl)Phenyl)Ethyl)-3,4-Dihydroisoquinolin-2(1H)-Yl)-N-Methyl-2-Phenylacetamide
NEBIDRAZINE
L-Histidine, Hydrochloride (1:1)
YM178
NIFURTOINOL
IMC-RON8
Pediatric Psychiatric Disorder
Early Fetal Heart Rate Deceleration
Nightmare Disorder
A.F. Violet No. 1
Second Primary Cancer
CAM-3001
131I-MIBG
RUBITECAN
ZIO-301
EMD 531444
rachitis
Ewing sarcoma family of tumors
lymphoplasmacytic lymphoma
Prothyroliberin Release
ovarian low malignant potential tumor
Nitalapram
KM8761
Varlitinib
Poliovirus Type 1 Antigen (Formaldehyde Inactivated)
POLIOVIRUS TYPE 2 ANTIGEN (FORMALDEHYDE INACTIVATED)
Poliovirus Type 3 Inactivated Antigen, B
PINUS ELLIOTTII POLLEN
PINUS MONTICOLA POLLEN
Anti-Epidermal Growth Factor Receptor Monoclonal Antibody IMC-11F8
Sulfogaiacol
Lagociclovir
LAGOCICLOVIR
DTaP
Anti-Nucleolin Aptamer AS1411
Dual PI3 Kinase/mTOR Inhibitor PKI-587
Survivin mRNA Antagonist EZN-3042
Late Fetal Heart Rate Deceleration
Late Deceleration
FD and C Violet No. 1
Pergacid Violet 3B
Tertracid Brilliant Violet 6B
Alpha Thalassemia, Severe Disease
PI3K Inhibitor ZSTK474
VEGFR/FGFR Dual Kinase Inhibitor E-3810
Visilizumab
Nutritional Disorder
Hashimoto thyroiditis
autoimmune thyroiditis
hypospadias
Diamond-Blackfan anemia
congenital pure red cell aplasia
erythrogenesis imperfecta
inherited erythroblastopenia
Kostmann disease
CRLX101
R788 sodium
MET Tyrosine Kinase Inhibitor PF-02341066
OE 312
Irosustat
AMG 403
PINUS PALUSTRIS POLLEN
PINUS SYLVESTRIS POLLEN
(+/-)-3-(p-Methylbenzylidene)Camphor
B01AB10
Berberinum Chloride
EINECS 200-999-5
Necitumumab
IMC-11F8
NK 204
Early Deceleration
Multi-Kinase Inhibitor E7080
(R)-(2,3-Dimethoxyphenyl)(1-(2-(4-Fluorophenyl)Ethyl)Piperidin-4-Yl)Methanol
TALASTINE HYDROCHLORIDE
BMS 936564
gemcitabine hydrochloride
SKF 284
Chronic Lymphocytic Thyroiditis
EFTs
sulfonamide
kidney failure
Central Nervous System Primitive Neuroectodermal Tumor (WHO Grade IV)
Blackfan-Diamond anemia
congenital neutropenia
Raftilose Synergy 1
Chinese Cinnamon Oil
Cinnamomum Cassia Oil
AP24534 HCl
EZN-2285
PP-105
PINUS RIGIDA POLLEN
PINUS THUNBERGII POLLEN
PLATANUS HYBRIDA POLLEN
Coagulation Factor IX Complex Human
LDE225
RMI 10,482A
Phonological Disorder
(E)-N(1)-(3-(dimethylamino)propyl)-N(8)-hydroxy-2-((naphthalene-1-loxy)methyl)oct-2-enediamide
RU 2341
AF Violet No. 1
Pergacid Violet 2B
Second Primary Malignant Neoplasm
Prolactin Releasing Factor Activity Alteration
Cinnamomum Aromaticum Oil
Microtubule Inhibitor EPC2407
Steroid Sulfatase Inhibitor BN 83495
Poliovirus Type 1 Inactivated Antigen, B
Trastuzumab-MCC-DM1
acetyl-L-carnitine
(1S,4S)-(6-Dimethylamino-4,4-Diphenyl-Heptan-3-Yl) Acetate
Benzeneethanol, B-[2-(Dimethylamino)Propyl]-.Alpha.-Ethyl-.Beta.-Phenyl-, Acetate (Ester), (-)-
Surinabant
FERUMOXYTOL NON-STOICHIOMETRIC MAGNETITE
TEGLICAR
Factor IX Complex
NECITUMUMAB
Akt Inhibitor MK2206
TAK-700
Amphecloral
OPAVIRALINE
Nifurtoinol
Jet Lag Type Circadian Rhythm Sleep Disorder
Formyl Violet S4BN
Polaxal Violet 6B
Gastrointestinal System Dysplasia
Brovanexine Hydrochloride
MT111
4-OHT
Prociclide
mifamurtide
DBA
genetic infantile agranulocytosis
infantile genetic agranulocytosis
BcI-2 Family Protein Inhibitor ABT-263
CHINESE CINNAMON OIL
MPC-4326
Ultralow-Molecular-Weight Heparin AVE5026
Trastuzumab-MCC-DM1 Antibody-Drug Conjugate
Rubella Infection
Histidine Hydrochloride, L-
Teglicar
(3R)-3-((Tetradecylaminocarbonyl)Amino)-4-(Trimethylazaniumyl)Butanoate
Gamma-Secretase Inhibitor RO4929097
HDP-Cidofovir
Amfecloral
LEXIDRONAM
Chinese Herbal Formulation PHY906
WEE1 Inhibitor MK-1775
BENZYL VIOLET
11386 Violet
Fast Acid Violet 5BN
Solar Violet 5BN
2-(2-(Dimethylamino)Ethyl)-4-(Phenylmethyl)-1(2h)-Phthalazinone Hydrochloride
Upset
LYSINE MONOHYDRATE
L-Lysine Monohydrate
Autoimmune Gastritis
Adult Polycystic Kidney Disease Type 2
Arnold Chiari Malformation, Type II
Cancer, Cervix
Chromosome 6 Linked Autosomal Recessive Parkinsonism
Hemihydrate Apomorphine Hydrochloride
Hydrochloride, Hemihydrate Apomorphine
Hyperimmunoglobulin E Recurrent Infection Syndrome
Ischemic-Hypoxic Encephalopathies
Kidney Dysplasia, Multicystic
Kidney Dysplasias, Multicystic
Multicystic Dysplastic Kidney
Multicystic Dysplastic Kidneys
Multicystic Kidney Dysplasia
Multicystic Kidney Dysplasias
Multicystic Kidneys
PHOTOCONVULSIVE REACTION
FANCONI RENOTUBULAR SYNDROME
SPONDYLOEPIPHYSEAL DYSPLASIA, OMANI TYPE
CDMD
OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS
Homocysteinemia
CATARACT, CONGENITAL, X-LINKED
NEPHROTIC SYNDROME, TYPE 2
CONVULSIONS, BENIGN FAMILIAL INFANTILE, 1
LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO
IWC
MFM3
CDGII/COG1 CEREBROCOSTOMANDIBULAR-LIKE SYNDROME
FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED
SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS
Bulbar palsy
FANCA
HYDATIDIFORM MOLE
BLCPMG
46,XX SEX REVERSAL 1
46,XX SEX REVERSAL, SRY-POSITIVE
XX MALE, SRY-POSITIVE
PSEUDOHERMAPHRODITISM, FEMALE, DUE TO PLACENTAL AROMATASE DEFICIENCY
LIPOMATOSIS, FAMILIAL BENIGN CERVICAL
FML
DERMATOFIBROSIS LENTICULARIS DISSEMINATA, ISOLATED
ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS
FANCONI ANEMIA, COMPLEMENTATION GROUP A
FANCONI ANEMIA
BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA
46,XX TRUE HERMAPHRODITISM, SRY-POSITIVE
APLD
NF1 MICRODUPLICATION SYNDROME
PHOTOSENSITIVITY
EPILEPSY, PHOTOGENIC
FRTS1
HSN1A
SUPRANUCLEAR PALSY, PROGRESSIVE, 1, ATYPICAL
SRXX1
SRXY3
AROMATASE DEFICIENCY
HSD
LIPOMATOSIS, FAMILIAL MULTIPLE
HSN IA
CMH
HTX5
CATARACT, CONGENITAL TOTAL, WITH POSTERIOR SUTURAL OPACITIES IN HETEROZYGOTES
OVOTESTICULAR DISORDER OF SEX DEVELOPMENT
DISORDERED STEROIDOGENESIS DUE TO CYTOCHROME P450 OXIDOREDUCTASE DEFICIENCY
LONG QT SYNDROME 2, ACQUIRED, SUSCEPTIBILITY TO
MYOTONIC DYSTROPHY 1
HSAN1A
NEUROPATHY, HEREDITARY SENSORY RADICULAR, AUTOSOMAL DOMINANT, TYPE 1A
Umbilical cord bleeding
HYDM
CHM
PSEUDO-TORCH SYNDROME
OVOTESTICULAR DSD
46,XX GONADAL DYSGENESIS, COMPLETE, SRY-POSITIVE
CHROMOSOME 2q37 DELETION SYNDROME
HYPERHOMOCYSTEINEMIA
ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR
CRIE
46,XY SEX REVERSAL 3
DISORDERED STEROIDOGENESIS DUE TO POR DEFICIENCY
FANCONI RENOTUBULAR SYNDROME 1
FRTS
DM1
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA
CXN
ICHTHYOSIS WITH CONFETTI
ICHTHYOSIS VARIEGATA
OBESITY, SUSCEPTIBILITY TO
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO CYTOCHROME P450 OXIDOREDUCTASE DEFICIENCY
MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA, SUSCEPTIBILITY TO
HUMEROSPINAL DYSOSTOSIS
CHONDRODYSPLASIA WITH MULTIPLE DISLOCATIONS
HSAN IA
NEUROPATHY, HEREDITARY SENSORY, TYPE IA
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1
PRDS
ACADVLD
ABS2
SEIZURES, BENIGN FAMILIAL INFANTILE, 1
MYOPATHY, MYOFIBRILLAR, 3
Type II Arnold Chiari Malformation
Vaccine, DTwP
WAY-VPA-985
aluminum chloride, anhydrous
Carcinoma of corpus uteri
Neoplasm of abdominal wall
Abdominal wall tumor
Malignant epithelial neoplasm of body of uterus
Multicystic Kidney
spadon
Cancer, Sigmoid
DTwP Vaccine
Dysplasia, Multicystic Kidney
Dysplasias, Multicystic Kidney
Encephalopathy, Ischemic-Hypoxic
Diathesis, Cystine
Syndrome, Moeschler Clarren
Dysplasias, Oculoauriculovertebral
Disability, Intellectual
Limb Pain, Phantom
Angina, Stable
Anginas, Chronic Stable
Chronic Stable Anginas
Talipe
Dysplasia, Oculoauriculovertebral
Oculoauriculovertebral Dysplasias
Oculoauriculovertebral Spectrums
Pain, Phantom Limb
Bleeding, Vaginal
Stable Angina Pectoris
Cystine Storage Disease
Diseases, Cystine Storage
Diatheses, Cystine
Disease, Goldenhar
Pains, Phantom Limb
Anginas, Stable
1-(2-methoxyethyl)-2-methyl-4,9-dioxo-3-(pyrazin-2-ylmethyl)-4,9-dihydro-1H-naphtho(2,3-d)imidazolium bromide
Storage Diseases, Cystine
Hemolytic Anemia Due to G6PD Deficiency
Oculoauriculovertebral Spectrum
Facioauriculovertebral Sequences
Intellectual Disability
Pains, Phantom
Platelet Fibrinogen Receptor, Deficiency of
Embonate, Triptorelin
Stable Angina
Stable Angina, Chronic
Pectori, Stable Angina
Insulins
Cystine Diseases
Oculoauriculovertebral Dysplasia
Phantom Limb Pains
Chronic Stable Angina
Cystine Storage Diseases
Cystine Diatheses
Limb Pains, Phantom
Pain, Phantom
Phantom Pains
Katayama Fever
Bleedings, Vaginal
Stable Anginas, Chronic
Stable Angina Pectori
monoclonal antibody CNTO 328
Cystine Disease
Cystine Diathesis
Moeschler Clarren Syndrome
Facioauriculovertebral Sequence
Fever, Katayama
Selective Serotonin Reuptake Inhibitors
Stable Anginas
Angina Pectoris, Stable
Angina Pectori, Stable
Pectoris, Stable Angina
Talipes
Disease, Cystine Storage
Storage Disease, Cystine
Goldenhar Disease
Vaginal Bleedings
Angina, Chronic Stable
SNDX-275
azzalure
bocouture
vistabel
Swelling of structure of eye
10-acetoxy-10,11-dihydro-5H-dibenz(b,f)azepine-5-carboxamide
Coronary Culprit Lesion
Hereditary Hageman Factor Deficiency
XAN-02
Aurora Kinase Inhibitor AS703569
ARO-002
Lytispasm
Hepatitis B Virus Subtype ADW HBsAg Surface Protein Antigen
Tubulin Inhibitor CYT997
Recombinant Somatotropin
Varicella Zoster Infection
IRAP
Hereditary Factor X Deficiency
Hereditary Fibrin Stabilizing Factor Deficiency
Intestinal Duplication
Vitamin K Deficiency
Normal Pupillary Response
Eye Finding
Endovalpin
2-benzofurancarboxamide, 3-((dimethylamino)methyl)-n-(2-(4-((hydroxyamino)carbonyl)phenoxy)ethyl)-
Aluminum Chloride Anhydrous
BRAF Inhibitor GSK2118436
ALK1-Fc Fusion Protein ACE-041
Angiopoietin 1/2-Neutralizing Peptibody AMG 386
Adult Rickets
Dipeptidyl Peptidase-4 Inhibitor
IL-1RN
IL1 Inhibitor
Intracellular Interleukin-1 Receptor Antagonist
Autosomal Dominant Inherited Disorder
Radial Hypoplasia
BRAF(V600E) Kinase Inhibitor RO5185426
Abexinostat
ABEXINOSTAT
Anthrax Vaccine Adsorbed
Rh Immune Globulin
AbobotulinumtoxinA
Thrombophilia
FLA 136
4-(5-(Pyridin-4-yl)-1h-1,2,4-triazol-3-yl)pyridine-2-carbonitrile
adult rickets
NRTI
ICIL-1RA
Esophageal Duplication
Pena-Shokeir Syndrome
Hereditary Factor XII Deficiency
Congenital Cardiovascular Disorder
KD019
3-((dimethylamino)methyl)-N-(2-(4-(hydroxycarbamoyl)phenoxy)ethyl)-1-benzofuran-2-carboxamide
Gondafon
Hepatitis A Virus Inactivated Antigen, B
Hepatitis B Virus Surface Protein Antigen, B
SCH 900105
Topiroxostat
Nucleoside Reverse Transcriptase Inhibitor
Stuart-Prower Factor Deficiency
Immunoglobulin A
Hepatitis A Virus Strain CR 326F Antigen (Formaldehyde Inactivated)
SU 20
SPM 927
IL-1ra
Juvenile Hyaline Fibromatosis
Molluscum Fibrosum
5 Alpha Steroid Reductase 2 Deficiency
Benign Melanocytoma
Myelocele
Porencephalic Cyst
Pulmonary Artery Stenosis
Thalidomide-Induced Birth Defect
Steroid 5-alpha-reductase Inhibitor
LYMPHOSARCOMA, MALIGNANT
(8R)-3alpha-Hydroxy-8-isopropyl-1alpha H,5alphaH-tropanium Bromide (+-)-tropate Monohydrate
HSDB 7438
HMR1726
IncobotulinumtoxinA
ADD 234037
ARRY-162
Nucleoside Analog Reverse Transcriptase Inhibitor
Anti-IL9 Monoclonal Antibody MEDI-528
Drotin
DPP-4 Inhibitor
Interleukin-1 Receptor Antagonist Protein
Intracellular IL-1 Receptor Antagonist Type II
Mesenchymal Dysplasia
Glucobay
Hereditary Factor I Deficiency
Mitral Valve Atresia
Penile Agenesis
Retinopathy of Prematurity Stage 3 Ridge with Extraretinal Fibroblastic Proliferation
Dexanabinol
DRG-0246
Androgen Resistance Syndrome
Sulfonamide Anti-Infective Agent
gamma-Hydroxybutyrate
LPFB
HDAC Inhibitor PCI-24781
Trebananib
Neuropathic Pain
GENZ 99067
Cytoplasmic Vacuolation
Toxoid Vaccine
Non-nucleoside Reverse Transcriptase Inhibitor
3-Methylglutaconic Aciduria
Hereditary Factor XIII Deficiency
Pulmonary Valve Atresia with Intact Ventricular Septum
Pulmonary Valve Atresia with Ventricular Septal Defect
Dextro-Transposition of the Great Arteries
Normal Ventricular Ejection Fraction
Congenital Abnormality of the Circulatory System
Uroepithelial Carcinoma
RG 7204
D2E7
(2S,3S)-3-((2-Methoxy-5-(5-(trifluoromethyl)-1H-tetrazol-1-yl)benzyl)amino)-2-phenylpiperidine
Oral JAK Inhibitor INCB18424
MEK Inhibitor GSK1120212
NNRTI
Discordant Ventriculoarterial Connection
Duplicated Ureter
JOUBERT SYNDROME 12/15, DIGENIC
Metacarpal fusion
Overgrowth of the maxilla
Wolff-Parkinson-White ventricular preexcitation
BESTROPHINOPATHY, AUTOSOMAL RECESSIVE
SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME
Glomerulonephropathy
PACHD
Thick hair
Loss of visual fields
Thick skin
17-ALPHA-HYDROXYLASE/17,20-LYASE DEFICIENCY, COMBINED PARTIAL
Acholic stools
JWDS
FRAXE MENTAL RETARDATION SYNDROME
AVSD
AVCD
Venous stasis ulcer
HYPERCALCEMIA, INFANTILE
Immune deficiency
AVC DEFECT
JOUBERT SYNDROME 9/15, DIGENIC
Hypopigmentation of the iris
FTDALS
SCDO5
Vision loss
JAWAD SYNDROME
ATRIOVENTRICULAR CANAL DEFECT
Deficiency of coagulation factors
ECYT1
AMELOGENESIS IMPERFECTA, TYPE IE
PDHAD
ENDOCARDIAL CUSHION DEFECT
Calcifications
Intellectual disability
BDPLT1
MAPLE SYRUP URINE DISEASE, TYPE III
MICROCEPHALY WITH MENTAL RETARDATION AND DIGITAL ANOMALIES
LUNG AGENESIS
3M SYNDROME
Premature ventricular contraction (PVC)
AI1E
Sleeping disturbances
ATRIOVENTRICULAR SEPTAL DEFECT
Increased fibrinolysis
Dementia, frontal lobe
Mitral valve atresia
Coloboma, iris
SFPKS
PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY
Neuropathic pain
Edodekin Alfa
Infections, Respirovirus
Lu-Tex
Respirovirus Infections
Metamizole sodium
Hypermetria
Responds to pain
Danubian Endemic Familial Nephropathy
Maltreatment, Child
Syndromes, Twin-to-Twin Transfusion
Immune Thrombocytopenic Purpura
Familial Hyperinsulinemic Hypoglycemia 1
3'-((2-((2-(3-chlorophenyl)-2-hydroxyethyl)amino)ethyl)amino)-(1,1'-biphenyl)-3-carboxylic acid
Dysencephalia Splanchnocystica
Sialidosis, Type II
Hypotransferrinemia, Familial
cardionogen-2
TCSOX229
Fetal Transfusion Syndrome
Syndromes, Fetal Transfusion
Transfusion Syndromes, Fetal
Fetofetal Transfusion Syndrome
Twin to Twin Transfusion Syndrome
Twin Twin Transfusion Syndrome
Hypoglycemias, PHHI
PHHI Hypoglycemias
Aminobenzoates
angiotensin II-(1-7)
afobazole
CMT 2I
Meckel-Gruber Syndrome
Asphyxiating Thoracic Dystrophy 3
Cerebral Amyloid Angiopathy, App-Related
Arcc2
Mistreatment, Child
Twin-to-Twin Transfusion Syndrome
Transfusion Syndrome, Twin-to-Twin
Twin-to-Twin Transfusion Syndromes
Hyperinsulinisms, Congenital
Infancy Hyperinsulinemia Hypoglycemias
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2l
Meckel Syndrome, Type 1
Potter Syndrome
Amyloidosis, Cerebroarterial, App-Related
vuc198
Fetofetal Transfusion Syndromes
Transfusion Syndrome, Fetofetal
Visual Impairment
Impairments, Visual
Visual Impairments
Congenital Hyperinsulinisms
Persistent Hyperinsulinemia Hypoglycemia of Infancy
Hyperinsulinism, Congenital
Ectodermal Dysplasia, Type 4
vuc247
Child Mistreatment
Bickel Syndrome, Fanconi
Syndrome, Fetal Transfusion
Transfusion Syndromes, Fetofetal
Impairment, Visual
Thrombocytopenic Purpura, Autoimmune
Charcot-Marie-Tooth Neuropathy, Axonal, Type 2l
Cmt2l
Cerebral Amyloid Angiopathy, App-Related, Iowa Variant
Cataract, Age-Related Cortical, 2
CDNG3
Child Maltreatment
Myotubular Myopathy 1
Congenital Hyperinsulinism
Meckel-Gruber Syndrome, Type 1
Cerebral Amyloid Angiopathy, App-Related, Flemish Variant
Granulomatous Enteritis
Transfusion Syndrome, Fetal
Dihydropyrimidinurias
Glycerate Kinase Deficiency
Meckel Syndrome
Kfsdx
Keratosis follicularis spinulosa decalvans
cardionogen-3
Fanconi Bickel Syndrome
Syndrome, Fanconi Bickel
Fetal Transfusion Syndromes
Syndrome, Fetofetal Transfusion
Syndromes, Fetofetal Transfusion
Syndrome, Twin-to-Twin Transfusion
Transfusion Syndromes, Twin-to-Twin
Zlotogora-Ogur syndrome
Stickler Syndrome, Type I
Cerebral Amyloid Angiopathy, App-Related, Arctic Variant
Cerebral Amyloid Angiopathy, App-Related, Italian Variant
CDNG2
Dowling-Degos-Kitamura Disease
Multicore Myopathy With External Ophthalmoplegia
Multiminicore Myopathy
Nystagmus, Infantile Periodic Alternating, X-Linked
Radioulnar Synostosis with Microcephaly, Short Stature, Scoliosis, and Mental Retardation
Generalized Resistance To 1,25-Dihydroxyvitamin D
Dysplastic Nevus Syndrome, Hereditary
PK Deficiency
Nevus, Epidermal
Axenfeld-Rieger Syndrome, Type 1
Erythrocytosis, Familial, 1
Multiminicore Disease With External Ophthalmoplegia
Spondyloepiphyseal Dysplasia, Late
Vitreoretinochoroidopathy dominant
Cutis Laxa, Autosomal Recessive
stavudine, lamivudine, nevirapine drug combination
Jawad Syndrome
Frontotemporal Dementia With Motor Neuron Disease
Vitreoretinochoroidopathy, Autosomal Dominant
Bifid Nose, Autosomal Recessive
Cystinosis, Infantile Nephropathic
Nevus, Keratinocytic, Nonepidermolytic
Hypobetalipoproteinemia, Familial, 1
Dentinogenesis Imperfecta 1
Reticular Pigment Anomaly of Flexures
Dysplasminogenemia
Melanoma, Familial
Fammm
MODY, Glucokinase-Related
Cataract, Autosomal Recessive Congenital 1
Nasal Cartilages, Agenesis of
Pelviureteric Junction Obstruction
Habsburg Jaw
Minicore Myopathy
Deafness, X-Linked 3
Deafness, X-Linked 4, Congenital Sensorineural
Vitreoretinochoroidopathy, Autosomal Dominant, With Nanophthalmos
Hydronephrosis Due To Pujo
Myofibromatosis, Juvenile
Atrial Septal Defect, Primum Type
Pyruvate Kinase Deficiency of Red Cells
Sweating, Cold-Induced
Familial erythrocytosis, 1
Erythrocytosis autosomal dominant benign
Cataract, Punctate, Progressive Juvenile-Onset
Dowling-Degos Disease
Minicore Myopathy with External Ophthalmoplegia
Multicore Myopathy
Neurosensory Nonsyndromic Recessive Deafness 4
Deafness, Autosomal Recessive 4
Glomus Tumors, Familial, 3
Tsukahara Syndrome
Polydactyly, Postaxial, Type A1
Hapsburg Jaw
DOOR Syndrome
Frontotemporal Dementia-Amyotrophic Lateral Sclerosis
Cataract, Congenital, Cerulean Type, 4
Vertigo, Benign Recurrent
Vitamin D-Resistant Rickets With End-Organ Unresponsiveness To 1,25-Dihydroxycholecalciferol
Postaxial Polydactyly, Type A
RGH-188
Rieger Syndrome, Type 1
Erythrocytosis familial, 1
oleic acid methyl ester
imetelstat
Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia
Rickets, Hereditary Vitamin D-Resistant
Hypocalcemic Vitamin D-Resistant Rickets
Familial Atypical Mole-Malignant Melanoma Syndrome
MODY, Type 2
stavudine - lamivudine - nevirapine
Juvenile Polyposis, Infantile
Juvenile Polyposis Of Infancy
Ichthyosis, Follicular Atrophoderma, Hypotrichosis, and Hypohidrosis
Prognathism, Mandibular
German Syndrome
Hypobetalipoproteinemia, Normotriglyceridemic
Capdepont Teeth
Dystonia 1, Torsion, Autosomal Dominant
Candidiasis, Familial Chronic Mucocutaneous
'Turban Tumor' Syndrome
Split-Foot Deformity With Mandibulofacial Dysostosis
Early-Onset Torsion Dystonia
Candidiasis, Familial, Type 4
Pearson Marrow-Pancreas Syndrome
SCID Due to ADA Deficiency
Cytomegalic Adrenocortical Hypoplasia
Ceroid Lipofuscinosis, Neuronal, 8
Pearson's marrow-pancreas syndrome
Patterson-Stevenson-Fontaine Syndrome
Dystonia Musculorum Deformans 1
Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism
Sideroblastic anemia with marrow cell vacuolization and exocrine pancreatic dysfunction
Aniridia, Partial, with Unilateral Renal Agenesis and Psychomotor Retardation
ADA-SCID
CANDF4
Addison Disease, X-Linked
AHC with Isolated Gonadotropin Deficiency
Adrenal Hypoplasia, Congenital
Developmental phonological disorder
Aspirin exacerbated respiratory disease
Tobacco use
Primary degenerative dementia
Obsessional personality disorder
Phonological (speech) disorder
Lamellar cataract
Visual field loss
Decreased coagulation factors
Microcephaly
Bone marrow failure
Multicystic dysplastic kidney
HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2
Generalized edema
DFNB10
EEG shows burst suppression pattern
ECTD10A
Narrow palpebral fissures
Methylmalonic aciduria
Cutis aplasia of scalp
PBD7A
Multicystic dysplastic kidneys
Decreased head circumference
Hairy elbows
UROLITHIASIS, 2,8-DIHYDROXYADENINE
PCC
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1
SELECTIVE T-CELL DEFECT
ACML
Idiopathic thrombocytopenia purpura
AOVD1
LI1, FORMERLY
APRT DEFICIENCY
UROLITHIASIS, DHA
Coloboma of iris
Zonular cataract
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT
Ventricular dilatation
Increased T4
STCD
Visual field defects
NCIE1, FORMERLY
MANSB
Night blindness, congenital stationary, complete
AORTIC VALVE DISEASE 1
Small head circumference
PAPA1
ADENINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY
HH7
Dilated ventricles
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
HYC1
Ischemic heart disease
Prolonged activated partial thromboplastin time
Adie pupil
Generalized weakness
Weakness, generalized
Thickening of stratum corneum
3-methylglutaconic aciduria
CG14
Narrowing of retinal blood vessels
COPD
BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES
Multicystic kidneys
LEUKEMIA, CHRONIC MYELOID, ATYPICAL
NEPHROLITHIASIS, DHA
Hypochloremia
ECTD10B
SHCB
Precocious puberty, gonadotropin-independent
APRTD
CCA3
HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA
EDA
ARCI2
ARCI1
Bifid ureter
DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
Reduced head circumference
PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER)
PREMATURE VENTRICULAR COMPLEXES UNIFOCAL
CIGB-300
(+/-)-Noradrenaline
Avagraf
Norepinephrine
Advagraf
Ovarian tumors of low malignant potential
XM22
Premature Ventricular Complexes Interpolated
Follicle Stimulating Hormone Beta Subunit
Congenital Anomaly of Cardiovascular System
Carbonate Ion
RimabotulinumtoxinB
Neoplastic Disease
Ma Huang
TPH Inhibitor LX1606
Follitropin Beta Chain
Ovarian tum. of low malig. poten.
Rimabotulinumtoxinb
CK2-targeting Synthetic Peptide CIGB-300
LX1606 Hippurate
Infant Failure to Thrive
Ephedrae Herba
Ferrosoferric Oxide
Proteasome Inhibitor ONX 0912
Endocardial Cushion Defect
Juniperus oxycedrus Leaf Oil
Tbo-filgrastim
Centelase
Ephedra Sinica Extract
STREPTOCOCCUS PNEUMONIAE TYPE 4 CAPSULAR POLYSACCHARIDE DIPHTHERIA CRM197 PROTEIN CONJUGATE ANTIGEN
HDFN
OMP-54F28
Tryptophan Hydroxylase Inhibitor LX1606
TREBANANIB
Common Atrioventricular Canal
LX1032 Hippurate
Carbonate
Ado Trastuzumab Emtansine
HIE
Lacks Energy
Hyperextension of Knee Deformity
APC
Streptococcus pneumoniae Type 4 Polysaccharide Conjugate Antigen, A
Acute ST Elevation Myocardial Infarction by ECG Finding
(2E,4E,6E,10E)-3,7,11,15-Tetramethylhexadeca-2,4,6,10,14-Pentaenoic Acid
Cymidon
3,3',5,5'-Tetrabromo-2,2'-biphenyldiolmono(dihydrogen phosphate)
Ephedra sinica Stem
Follitropin Subunit Beta
Follicle Stimulating Hormone, Beta Polypeptide
Common AV Canal
Ketodur
Norepinephrine, DL-
Potassium Alum
Venous Obstruction
Old Myocardial Infarction by ECG Finding
Iron (II, III) Oxide
Blocked Ventricular Premature Complex
Genu Recurvatum
Juniper Oil
Meruvax II
Unifocal Ventricular Premature Complex
1,2-benzenediol, 4-(2-amino-1-hydroxyethyl)-, (+/-)-
LX1606
VLCAD
PAC
Hypertensive chronic kidney disease
Chronic kidney disease due to hypertension
Type I, HSN
docetaxel hydrate
Enthesitis Related Arthritis, Juvenile
Hereditary Sensory and Autonomic Neuropathy Type 1
Syndrome, HIE
HSN Type I
Myopathies, X-Linked Myotubular
Familial Hyperinsulinisms
Hereditary Sensory Neuropathy Type 1
Job Buckley Syndrome
HIE Syndrome
Hereditary Sensory Neuropathy Type I
Centronuclear Myopathies, X-Linked
Myopathies, X-Linked Centronuclear
Neuropathy, Hereditary Sensory And Autonomic, Type I
X-Linked Myotubular Myopathy
Familial Hyperinsulinism
Job Syndrome
X-Linked Centronuclear Myopathy
Familial Afibrinogenemia
Job-Buckley Syndrome
S Methylmethionine
Xlmtm
Myopathy 1, Myotubular
Hereditary Sensory Neuropathy Type Ia
Myopathy, X-Linked Centronuclear
X-Linked Myotubular Myopathies
Infancy Hyperinsulinemia Hypoglycemia
Hypoglycemias, Persistent Hyperinsulinemic
Buckley Syndrome
Syndrome, Buckley
Hyperinsulinism, Familial
HSAN 1
Hyperinsulinisms, Familial
Hereditary Sensory and Autonomic Neuropathy Type I
X Linked Centronuclear Myopathy
Job's Syndrome
Myotubular Myopathies, X-Linked
Hydrochloride, Histamine
Myopathy 1s, Myotubular
Job-Buckley Syndromes
X-Linked Centronuclear Myopathies
Hyperinsulinisms, Neonatal
N-debenzoyl-N-tert-butoxycarbonyl-10-deacetyltaxol
Myopathy, X-Linked Myotubular
Hyperinsulinemic Hypoglycemias, Persistent
Neonatal Hyperinsulinisms
Arthritis, Juvenile Psoriatic
Betamethasone 17-Valerate
HSAN Type I
Neuropathy, Hereditary Sensory Radicular, Autosomal Dominant
Persistent Hyperinsulinemic Hypoglycemias
Lansoprazole Abbot Brand
Congenital Afibrinogenemia
Craniofacial Dysostosis, Type 1; CFD1
Trisodium, Pentetate Zinc
Zinc Trisodium, Pentetate
Syndrome, Job-Buckley
Neuropathy Hereditary Sensory and Autonomic Type 1
Syndromes, Job
HSAN I
Neuropathy Hereditary Sensory Radicular, Autosomal Dominant
HIE Syndromes
Buckley Syndromes
Hereditary Sensory Autonomic Neuropathy, Type 1
Neuropathy, Hereditary Sensory, Type I
Persistent Hyperinsulinemic Hypoglycemia
Centronuclear Myopathy, X-Linked
Myotubular Myopathy 1s
Neonatal Hyperinsulinism
Syndrome, Job
Syndromes, HIE
Syndromes, Job-Buckley
azanone
Rickets, Adult
2-hydroxyflutamide
X Linked Myotubular Myopathy
Hypoglycemia, Persistent Hyperinsulinemic
Juvenile Psoriatic Arthritis
Hyperinsulinism, Neonatal
docetaxel trihydrate
Job Syndromes
Syndromes, Buckley
Type I, HSAN
Sepsis of newborn due to Streptococcus agalactiae
Blepharospasm (spasm of eyelid)
Dopa responsive dystonia
Maturity-onset diabetes of the young, type 5
Fetal or neonatal effect of medical induction of labor
MODY5
Finding of electrocardiogram U wave
ITP - Idiopathic thrombocytopenic purpura
Heritable pulmonary arterial hypertension
Tibial muscular dystrophy
Psychogenic seizures
Udd distal myopathy
Grass staggers
Very long chain acyl-coenzyme A dehydrogenase deficiency
Udd myopathy
Udd-Markesbery muscular dystrophy
Neoplasm
Grass tetany
Congenital hyperinsulinism
Tsh Deficiency
Monosomy 22q13
Thymidine Phosphorylase Deficiency
poly(sodium vinyl sulfonate)
Cholestasis, benign recurrent intrahepatic 1
Spastic Paraplegia 3a
Dohle leukocyte inclusions with giant platelets
Triphalangeal thumb polysyndactyly syndrome
Polydactyly, Preaxial II
Spastic Paraplegia Type 3a
Spastic Paraplegia 3
Methylmalonic Aciduria
L-2-Hydroxyglutaric Acidemia
Early-Onset Myopathy with Fatal Cardiomyopathy
Acyl-Coa Dehydrogenase Very Long Chain Deficiency
Encephalopathy, Petechiae, and Ethylmalonic Aciduria
disodium hydrogen phosphate anhydrous
Lactate Dehydrogenase Subunit Deficiencies
Fechtner syndrome
TPT and PSD syndrome
Familial Trichoepithelioma
Familial Juvenile Hyperuricemic Nephropathy 2
Salih Cmd
Methioninemia
dowling-degos disease
dark dot disease
Multicore Disease
Multiminicore Disease
Hereditary Arthro-Ophthalmopathy
Thyroid-stimulating hormone, deficiency of
Summerskill syndrome
Primary Torsion Dystonia
Early-Onset Generalized Torsion Dystonia
Autosomal Recessive Craniometaphyseal Dysplasia
Very Long-Chain Acyl Coenzyme A Dehydrogenase Deficiency
Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
Bidirectional Tachycardia Induced By Catecholamines
May-Hegglin anomaly
Dyt1
Oppenheim's Dystonia
Fluosol-DA
Polydactyly of Triphalangeal Thumb
Epstein syndrome
Multi-Minicore Disease
Cataract, Congenital Total
Pdgfra-Associated Myeloproliferative Neoplasm
Ren-Related Kidney Disease
Vlcad-C
Fechtner's syndrome
Cataract, total congenital
Epema Syndrome
Hereditary Arthro-Ophthalmo-Dystrophy
Thyroid-Stimulating Hormone Deficiency
Triphalangeal Thumb with Polysyndactyly
Vlcad-H
3-Oxoacid Coa Transferase Deficiency
Chronic Eosinophilic Leukemia
bexsero
Spg3a
Familial Amyloidosis, Finnish Type
Mitochondrial DNA Depletion Syndrome 1
3,3',5,5'-tetrabromo-2,2'-biphenyldiol mono(dihydrogen phosphate)
Minicore Disease
Oppenheim Dystonia
Telomeric 22q13 Monosomy Syndrome
Dermal Eccrine Cylindroma
Early-Onset Primary Dystonia
Pdgfra-Associated Chronic Eosinophilic Leukemia
Salih Myopathy
Bietti Crystalline Retinopathy
Triphalangeal Thumb-Polydactyly Syndrome
Kymenlaakso Syndrome
Familial Amyloid Polyneuropathy Type Iv
Salih Congenital Muscular Dystrophy
Acadvl
Gelsolin-Related Amyloidosis
bromofenofos
FSH beta
FSH, beta Chain
FSH, beta Subunit
Follicle Stimulating Hormone, beta Polypeptide Chain
Follicle Stimulating Hormone, beta Subunit
Follicle-Stimulating Hormone, beta Subunit
Narrowed palpebral fissures
SWNTS1
PVOD1
SRPS3
PAN
Central apnea
BECTS
PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT
SMITH-MCCORT DYSPLASIA 1
SYM1
Right heart failure
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID
RHPD1
CATARACT 40
SMC1
HMN2D
ADRENOMYELONEUROPATHY
SYM1A
Alveolar hypoventilation
BENIGN EPILEPSY OF CHILDHOOD WITH CENTROTEMPORAL SPIKES
Cortical visual impairment
SYMPHALANGISM, PROXIMAL, 1A
CATARACT 17, MULTIPLE TYPES
Inflammatory infiltrate
CATARACT 21, MULTIPLE TYPES
CTRCT17
CAPILLARY MALFORMATIONS, CONGENITAL
CTRCT40
Question mark ears
SCHWANNOMATOSIS 1
CATARACT 5, MULTIPLE TYPES
Visual field defect
CMC
CTRCT21
CTRCT5
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1
Intrahepatic biliary atresia
CATC1
Atresia of the external auditory canals
LDS1
ACETABULAR DYSPLASIA
LOEYS-DIETZ SYNDROME 1
AAT5
Hypermobility of joints
DHMN2D
4-Hydroxyandrost-4-ene-3,17-dione
Hyperinsulinemia
Cushing Disease
I have a lack of energy
Failure to Thrive
6-Acetyl-8-cyclopentyl-5-methyl-2-((5-(piperazin-1-yl)pyridin-2-yl)amino)-8h-pyrido(2,3-d)pyrimidin-7-one
Acute ST Elevation Myocardial Infarction by EKG Finding
N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-5-(ethyl(tetrahydro-2H-pyran-4-yl)amino)-4-methyl-4'-(morpholinomethyl)-[1,1'-biphenyl]-3-carboxamide
Elevated Transaminases
17Alpha-Hydroxyprogesterone
Inappropriate Sinus Tachycardia by EKG Finding
Atrioventricular Nodal Reentry Tachycardia by ECG Finding
BRAF(V600E) Inhibitor CEP-32496
Atrioventricular Nodal Reentry Tachycardia by EKG Finding
4-Amino-1-((1S,4R,5S)-2-fluoro-4,5-dihydroxy-3-(hydroxymethyl)cyclopent-2-en-1-yl)pyrimidin-2(1H)-one
Paroxysmal Supraventricular Tachycardia by ECG Finding
Type 3 Hypersensitivity Reaction
Atrial Premature Complex by ECG Finding
Delta(4)-Pregnene-17Alpha-Ol-3,20-Dione
Paroxysmal Supraventricular Tachycardia by EKG Finding
Alpha Hydroxy Progesterone
Rituximab Biosimilar BI 695500
17OHP
Depigmentation
17-OH Progesterone
4-Hydroxyandrostenedione
Cushing's Disease
Primary Adrenal Insufficiency
Type III Hypersensitivity
Inappropriate Sinus Tachycardia
Lack Energy
Necrotizing Enterocolitis in Fetus or Newborn
ABP 980
Atrial Premature Complex by EKG Finding
DMS612
Fluorocyclopentenylcytosine
Muse (intraurethral alprostadil suppository)
Old Myocardial Infarction by EKG Finding
Paroxysmal Supraventricular Tachycardia
Secondary Hypogammaglobulinemia
TIC10
Palbociclib
AL3810
NSC 281612
Pregn-4-Ene-3,20-Dione, 17-Hydroxy-
Manganese, dichloro[(4aR,13aR,17aR,21aR)-1,2,3,4,4a,5,6,12,13,13a,14,15,16,17,17a,18,19,20,21,21a-eicosahydro-11,7-nitrilo-7Hdibenzo[b,h][1,4,7,10]tetraazacycloheptadecine-kN5,kN13,kN18,kN21,kN22]-, (PB-7-11-2344'3')-
Pustule
Trimebutine 3-Thiocarbamoylbenzenesulfonate
17-Hydroxypregn-4-Ene-3,20-Dione
Head and Neck Carcinoma
Cobimetinib
Inappropriate Sinus Tachycardia by ECG Finding
Autologous Sarcoma Cell Lysate
Inflammatory Infiltrate
Primitive Neuroectodermal Tumor
RG7446
RG7853
Nivolumab
17-Hydroxyprogesterone
Atrial Premature Complex
FF284
Type III Hypersensitivity Reaction
Lucitanib
4-Amino-Alpha-((Tert-Butylamino)Methyl)-3,5-Dichlorobenzyl Alcohol
Atrioventricular Nodal Reentry Tachycardia
DF 1681Y
Imisopasem Manganese
17alpha-Hydroxyprogesterone
BIBW 2992MA2
Alectinib
1-Naphthalenecarboxamide, 6-((7-((1-aminocyclopropyl)methoxy)-6-methoxy-4-quinolinyl)oxy)-n-methyl-
CR1447
NEC
finrozole
Sequelae of central nervous system tuberculosis
Undifferentiated spindle cell sarcoma
Familial benign hypercalcemia
Sequelae of genitourinary tuberculosis
AME - apparent mineralocorticoid excess
Sclerosing rhabdomyosarcoma
Refractory cytopenia of childhood
Acute myeloid leukemia with multilineage dysplasia
Pancreatic endocrine tumor, benign
Autosomal recessive Larsen syndrome
Undifferentiated round cell sarcoma
Pseudohypoaldosteronism type 2A
Noramidopyrine Methanesulphonate
Porencephalies
resotrans
Dermatofibrosarcoma Protuberans
Esmya
Protuberans, Dermatofibrosarcoma
Protuberan, Dermatofibrosarcoma
resotran
Pustular eruption
Succinate
First and second branchial arch syndrome
Juvenile onset Still's disease
Dermatofibrosarcoma
cobimetinib
obeticholic acid
Corticotropin
RTXM83
ABI-011
Factor 9
Glycopyrronium Bromide
Adrenocorticotropic Hormone
Plasma Thromboplastic Component
IDN 5404
RG7450
Marshall Syndrome
Plasma Thromboplastin Component
Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis Syndrome
Rituximab Biosimilar PF-05280586
PFAPA Syndrome
PTC
Rituximab Biosimilar RTXM83
Copanlisib
COSTOVERTEBRAL SEGMENTATION ANOMALIES
CATARACT 40 WITH OR WITHOUT MICROCORNEA
HYPERPHOSPHORYLATED PARATARG-7
BETA-MANNOSIDOSIS
HYPOCALCEMIA, FAMILIAL
NEURILEMMOMATOSIS, CONGENITAL CUTANEOUS
ANTERIOR SEGMENT ANOMALIES
GM1-GANGLIOSIDOSIS, TYPE I
HYPERTRICHOSIS CUBITI
STEINERT DISEASE
DYSTROPHIA MYOTONICA
GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1
RETINAL DYSTROPHY WITH EARLY MACULAR INVOLVEMENT
AMYLOIDOSIS, FAMILIAL, FINNISH TYPE
GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I
LYSOSOMAL BETA-MANNOSIDASE DEFICIENCY
HYDRONEPHROSIS DUE TO PUJO
DYSTROPHIA MYOTONICA 1
BETA-MANNOSIDASE DEFICIENCY
GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM
Autosomal dominant hypocalcemia
Cholate
Familial hypercalciuric hypocalcemia
CKD - chronic kidney disease
Dermatitis
Familial hypocalcemia
Level, Blood Alcohol
Fluticasone Salmeterol
Unilateral lobar pulmonary agenesis
Hypermethioninemia
Combination, Fluticasone-Salmeterol
ACRDYS1
Alcohol Level, Blood
Malacef
Acrodysostosis 2, with or without hormone resistance
Acrodysostosis 1 with or without hormone resistance;
Erythema migrans, lingual
Drug Combination, Fluticasone-Salmeterol
6-desoxy-6-methylenenaltrexone
ACRDYS2
Unilateral lung agenesis
Sodium, Risedronate
Combination, Fluticasone-Salmeterol Drug
Fluticasone Salmeterol Drug Combination
Porencephaly, Encephaloclastic
Fo-Shou-San
3-(3,4-dihydroxyphenyl)acrylic acid 2,2-dimethyl-8-oxo-3,4-dihydro-2H,8H-pyrano(3,2-g)chromen-3-yl ester
Fluticasone Salmeterol Combination
Antibody, D2E7
5-(4-methoxyphenyl)-3H-1,2-dithiole-3-thione
Scenesse
Experimental Organism Astrocytosis
Benoxinate hydrochloride + fluorescein sodium
Zoledronate
Onychomycosis caused by dermatophyte
Psoriatic Arthritis, Juvenile
Etomedac
Béfizal
Triflucan
Wellvone
Salofalk
Guillaine-Barre Syndrome
Abbot Brand of Lansoprazole
Encephaloclastic Porencephaly
Florisan N
Salazopyrin
Enthesitis-Related Arthritis, Juvenile
Paxtibi
Imizin
Hycamtamine
Landry-Guillain-Barre Syndrome
Bayotensin
Sugiran
Dinarkon
Prandase
Glucor
Trankimazin
Pentymal
Rho(D) Immune Human Globulin
benzyldimethyl(2-(2-(4-(1,1,3,3- tetramethylbutyl)-tolyloxy)ethoxy)ethyl) ammonium chloride
Droleptan
Ethiofos
Gammaphos
Allegron
Janssen Brand of Droperidol
Sigmoidal Cancer
Guillain-Barre Syndrome, Familial
Tham
Microval
Guillain-Barré Syndrome
Cross syndrome
Polyarthritis, Juvenile, Rheumatoid Factor Negative
Pyralin EN
Sigmoid Colon Cancer
Ozidia
Cancer of the Sigmoid
Difaterol
Breast Carcinoma
Misodine
Cancer of Sigmoid
Minprog
Eskazole
Viridal
Neuronox
((((1,1,3,3-tetramethylbutyl)cresoxy)ethoxy)ethyl)dimethylbenzylammonium chloride
Tafil
Hemifacial Microsomia
Ogastro
Pneumocystis carinii Pneumonia
Pneumocystosis
Pneumonia, Pneumocystis carinii
Pneumonia, Pneumocystis
Ag 3340
Cancer, Sigmoid Colon
Colon Cancer, Sigmoid
Deficiency, beta-Mannosidase
Hyperinsulinemia Hypoglycemia of Infancy
Hypoglycemia, PHHI
Nutritional Disorders
PHHI Hypoglycemia
Pneumocystis Pneumonias
Pneumonias, Pneumocystis
beta Mannosidase Deficiency
beta-Mannosidoses
beta-Mannosidosis
Duodenitis, Erosive
beta Mannosidosis
beta-Mannosidase Deficiencies
Dream anxiety disorder
Nightmare disorder
Infectious neuronitis
Recurring cold staphylococcal abscesses
Sulfonamide
Tardive dyskinesia
Nightmare
Nephrolithiasis
Unicameral bone cyst
Pneumonitis
Parasitic infectious disease
Ascending paralysis
Mountain sickness
Hydantoin
Reticulolymphosarcoma, diffuse
alpha-Amylase
Blepharospasm
Lassitude
Megacolon
Osteoarthrosis
Persistent hyperplasia of thymus
Psychosexual dysfunction
Acute infective polyneuritis
Tear film insufficiency
Male pattern alopecia
Subacute myeloid leukemia
Common baldness
Selective IgA immunodeficiency
Longitudinal deficiency of lower limb
Acholic stool
Avascular necrosis
Berger's disease
Debility
Edema, generalized
General weakness
Gluconic acid
Horner's syndrome
Hydroxyethyl starch
Impaired skin integrity
Ischemic necrosis
Methylbenzethonium chloride
Pyogenic arthritis
South African genetic porphyria
Total incontinence
Werlhof's disease
Abscess of bladder
Acholic feces
Anginal chest pain at rest
Aseptic leptospiral meningitis
CPS I deficiency
CPS deficiency
Cervical sympathetic paralysis
Chemical pneumonitis
Clay-colored stools
Colicky pain
Congenital hyperammonemia, type I
Cranial arteritis
Delta storage pool disease
Dilatation of colon
Dysmorphic sialidosis
Exudative pleurisy
FFH
Familial hypocalciuric hypercalcemia
Fetal giant
Fourth cranial nerve disorder
Gonococcal conjunctivitis neonatorum
Gonococcal ophthalmia neonatorum
Grey stools
Hematoporphyrinuria
Hereditary alopecia
Hereditary arthro-ophthalmopathy
Increased platelets
Infection by larvae of Trichinella spiralis
Isolated somatotropin deficiency
Isolated thyrotropic hormone deficiency
Isolated thyrotropin deficiency
Meconium ileus of the newborn
Mummified fetus
Nutritional disease
Paroxysmal choreoathetosis
Pink tooth
Potter syndrome
Prolonged rupture of membranes
Pseudomembranous enterocolitis in newborn
Pyridoxine responsive sideroblastic anemia
Recurrent hepatitis
Sialidosis, type 2
South African porphyria
Sponge kidney
Stricture of ureter
Superior oblique muscle innervation disorder
Thickening of skin
Tracheopathia osteochondroplastica
Trochlear nerve disorder
UROD deficiency
AVSD - Atrioventricular septal defect
Accessory thumb
Agenesis of nasal cartilages
Androgenetic alopecia
Angina at rest
Astrocytic cell proliferation
Astrocytic tumor of brain
Astrocytoma of brain
Atrioventricular septal defect
Atypical chronic myeloid leukemia
Autoimmune thrombocytopenic purpura
Axenfeld syndrome
Bathing trunk nevus
Black iron oxide
Capillary angioma
Central sleep apnea
Chromophobe adenocarcinoma
Chromophobe carcinoma
Congenital giant pigmented nevus
Congenital giant pigmented nevus of skin
Cytoplasmic vacuolation
Dabska's tumor
Daturine
Deep thrombophlebitis
Differentiated teratoma
Discordant ventriculoarterial connection with concordant atrioventricular connection
Disorder of nutrition
Disorder of trochlear nerve
Dorsal midbrain syndrome
Eccrine dermal cylindroma
Endovascular papillary angioendothelioma of childhood
Enostosis
Ethylphenylhydantoin
Factor IX complex preparation
Factor IX preparation
Fibromyxosarcoma
Gell and Coombs reaction type II
Generalized lentiginosis
Giant pigmented nevus
Giant pigmented nevus of skin
Glycogenase
Glycopyrronium
HDN - Hemolytic disease of the newborn
HES
Hemolytic disease of the newborn
Hereditary progressive arthro-ophthalmopathy
Horner syndrome
Hydroxyprogesterone preparation
Hypersensitivity reaction mediated by antibody
Increased serum protein level
Isolated TSH deficiency
Isolated growth hormone insufficiency
MCKD - Multicystic kidney disease
Male pattern baldness
Melanocytic nevus of skin
Memory dysfunction
Minimal change glomerulonephritis
Mitral valve dysplasia
Mucoid thickening of mitral valve
Multicystic kidney
Multicystic renal dysplasia
Neonatal gonococcal conjunctivitis
New growth
PKD - Polycystic kidney disease
Pattern baldness
Pigmented nevus of skin
Polycystic kidney disease
Sinus of Valsalva aneurysm
Spasm of eyelids
Staphylococcal toxic shock syndrome
Teratoma, differentiated
Thost-Unna keratoderma
Toxic pneumonitis
Tumor of thymus
Type II reaction
Velastatin
Abnormal phonology
Absent nose
Acute inflammatory neuropathy
Androgenic alopecia
Angle tumor
Asthenozoospermia
Beat to beat variability
Benign recurrent vertigo
Beta + thalassemia
Blood in vomit - symptom
Buckley's syndrome
Central sleep apnea syndrome
Depressive episode
Deviant phonology
Embden-Meyerhof pathway
Epithelioid malignant nerve sheath tumor
Erosion of skin
Eye and vision observations
Feeling weak
Giant cell fibroblastoma
Hypersensitivity reaction type II
Intellectual functioning disability
Intraretinal microvascular abnormality
Job-Buckley syndrome
Juvenile psoriatic arthritis
Kimmelstiel - Wilson disease
Low QRS voltages
NEC - Necrotizing enterocolitis
Nasal bridge wide
Necrotizing enterocolitis
Occupational dystonia
Oligoarthritis
Omenn's syndrome
Ophthalmological history and observations
Pathologic calcification
Perinatal necrotizing enterocolitis
Pertussis vaccine refused
Phonological disorder
Phonological impairment
Phonology disorder
Phonology impairment
Plantar grasp reflex
Polio immunization refused
Potter's anomaly of the kidney
Psychomotor fit
Quie-Hill syndrome
Renal tubulo-interstitial disease
Segawa dystonia
Sound system impairment
Tetanus immunization refused
Transient arthropathy of the shoulder region
Unable to swallow
Urine specific gravity low
Weakness - general
Perceived constipation
Anterior chamber angle tumor
CSA - Central sleep apnea
Autoimmune gastritis
Problem with balance
Cancer of cervix
MCGN - Minimal change glomerulonephritis
Megaureter due to congenital ureterovesical obstruction
Congenital obstructive megaureter
VFD - Visual field defect
IGHD - Isolated growth hormone deficiency
Skin depigmented
White vaginal discharge
PCK - Polycystic kidney disease
Drug-induced tardive dyskinesia
FHH - Familial hypocalciuric hypercalcemia
NG - New growth
Hypermobility of joint
Is informed
Range of joint movement increased
Knowledgeable
Mole of skin
Obstruction of vein
Occlusion of vein
Venous occlusion
Japanese encephalitis virus vaccine
3-Methylglutaconic aciduria
Selective immunoglobulin A deficiency
Acute post-infective radiculoneuropathy
Very long chain acyl-CoA dehydrogenase deficiency
VLCAD - Very long chain acyl-CoA dehydrogenase deficiency
Beta-D-mannosidosis
Beta-mannosidase deficiency
Bietti's crystalline retinopathy
CPS - Carbamoyl-phosphate synthase deficiency
Carbamoyl-phosphate synthase deficiency
Post-infectious polyneuritis
Deaf mutism
Idiopathic purpura
Pyoarthrosis
Neoplasm of thymus
Tobacco user
Hemophagocytic syndrome
CPNET
Carbamoyl-phosphate synthethase deficiency
Carbamoylphosphate synthetase I deficiency
Central primitive neuroectodermal tumor
Complement inhibitor
Complex partial seizure
Deficiency of glycerate kinase
Dental disease
Diffuse palmoplantar keratoderma of Thost-Unna
Disease related state
Excessive overactivity
Eye / vision finding
Fourth cranial nerve disease
Fourth heart sound, S>4<
Acute idiopathic polyneuritis
Acute idiopathic polyradiculoneuritis
Acute myeloid leukemia without prior myelodysplastic syndrome
Giant cell fibroblastoma of skin
Heterotopic calcification
Hypomagnesemic tetany
Impairment of balance
Increased insulin level
Increased purposeless goalless activity
Inflammatory disorder of digestive tract
Intellectual limitation
Intermediate and giant congenital nevus
Islet cell tumor, benign
Lymphosarcoma [obs]
Lymphosarcoma, diffuse [obs]
Melengestrol acetate preparation
Mesothelial neoplasm
Non-communicating hydrocephalus
Nonspeaking deaf
Nutritional disorder
Obstruction by kinking
Obstruction by torsion
Obstruction by twisting
Onychomycosis due to dermatophyte
Pathologically calcified structure
Primary malignant neoplasm of independent multiple sites
Rhabdomyomatous neoplasm
Rupture of amniotic sac 24 OR more hours before labor
Skin integrity impairment
Subacute granulocytic leukemia [obs]
Subacute monocytic leukemia [obs]
Subacute myelogenous leukemia [obs]
Subacute myeloid leukemia [obs]
Suppurative arthritis
T.I.N.
Thost-Unna diffuse palmoplantar keratoderma
Traumatic bone cyst
Trochlear nerve disease
Tubulointerstitial nephropathy
U wave - finding
Basal cell carcinoma, nodular
beta^+^ Thalassemia
Benzodiazepine
Acute inflammatory demyelinating polyradiculoneuropathy
Japanese B encephalitis vaccine
Distressed
Feeling upset
Bloody stool
TD - Tardive dyskinesia
Disease due to Respirovirus
Feeling distress
Level of loneliness
Loneliness level
Still's disease
Bleb
Neonatal alloimmune thrombocytopenia
ANT - Alloimmune neonatal thrombocytopenia
Alloimmune neonatal thrombocytopenia
Isoimmune neonatal thrombocytopenia
JRA - Juvenile rheumatoid arthritis
Juvenile rheumatoid arthritis
Juvenile seropositive arthritis
Dupuytren's disease
Eye/vision finding
Filtering bleb
Juvenile chronic arthritis, polyarticular seropositive
Juvenile idiopathic arthritis, polyarthritis, rheumatoid factor positive
Juvenile rheumatoid arthritis, seropositive
Juvenile seropositive polyarthritis
Convulsion
Marcain
dicalcium phosphate anhydrous
aplidin
Thymic Tumor
Thymus Tumor
CaHPO(4)
Co Translational Amino Acid Modification
Co Translational Protein Processing
Co-Translational Protein Modifications
Co-Translational Protein Processing
Cotranslational Protein Modifications
Cotranslational Protein Modification
Cotranslational Protein Processing
Modification, Co-Translational Protein
Modifications, Co-Translational Protein
Post Translational Amino Acid Modification
Post-Translational Amino Acid Modification
Posttranslational Amino Acid Modification
Processing, Co-Translational Protein
Protein Modification, Co Translational
Protein Modification, Co-Translational
Protein Modification, Cotranslational
Protein Modifications, Co-Translational
Protein Modifications, Cotranslational
Protein Processing, Co Translational
Protein Processing, Co-Translational
Protein Processing, Cotranslational
Roche Brand of Amitriptyline Hydrochloride
Thymic Tumors
Thymus Tumors
Tumor, Thymic
Tumor, Thymus
Tumors, Thymic
Amino Acid Modification, Co Translational
Amino Acid Modification, Post Translational
Amino Acid Modification, Posttranslational
Tumors, Thymus
Monocytosis
Cystadenofibroma
Abscess
ACTH
Adrenocorticotropin
Autoimmune Thyroiditis
B-Cell Leukemia
B-Lymphocytic Leukemia
Bone Marrow Fibrosis
Bone Tuberculosis
Ca-DTPA
Chondroitin
Christmas Factor
Dementia
Factor IX
Factor VIII
Factor VIII Related Antigen
Gonadal Dysgenesis
Gonadorelin
Hypospadias
IgA
Leukopenia
LH-RH
Lipomatosis
Lymphocytosis
Lymphopenia
Lymphoquin
Methylation
Minimal Change Glomerulonephritis
Neuroepithelioma
Oxytocin
Phosphorylation
Respiratory Distress Syndrome
Senescence
Spinal Neoplasms
Vaginitis
Viscum
von Willebrand Factor
CPT-11
TRP-2
Common Variable Immunodeficiency
Calcification
Blood Vessel Tumor
Neuroectodermal Tumor
Capillary Hemangioma
Hodgkin's Granuloma
Juvenile Rheumatoid Arthritis
Lymphocytic Thyroiditis
Pigmented Nevus
Plasma Cell Dyscrasia
Somnolence
Thyroid Extract
AL721
Chemical Pneumonitis
Coagulation Factor Deficiency
Anoxic encephalopathy
Collagenoma
D-His-6-Pro-8-NEt-LHRH
HPV-16 E6
Neoplasia
Ovalocytosis
PNET
Triploidy
Coagulation Factor IX
Coagulation Factor VIII
Mykrox
CIFN
Melan-A
Trisomy 13
Cushingoid
Obtundation
Trichothiodystrophy
Central Sleep Apnea Syndrome
Grade I Astrocytoma
Nasopharyngeal Cancer
Cancer of Nasopharynx
Cancer of the Nasopharynx
Hypoxic Encephalopathy
Hearing Loss
Papillary Meningioma
Carcinoma of Nasopharynx
Rubitecan
Trisomy 18
Monoclonal antibody 1D10
GANT
MART-1
OSM
RPI4610
aCML
Childhood Liver Cancer
Chordoma of Spinal Column
Chordoma of Spine
Chordoma of the Spinal Column
Coagulation Factor VIIIc
Collagen Hamartoma
Collagen Nevus
Colonic Mass
Congenital Cardiovascular Abnormality
Acquired Agammaglobulinemia
Congenital Cardiovascular Anomaly
Congenital Iodine Deficiency Hypothyroidism
Connective Tissue Nevus
Connective and Soft Tissue Finding
Cyst of Kidney
Cyst of Nasal Sinus
Cyst of the Kidney
Cyst of the Nasal Sinus
Acute Infective Polyneuritis
Dental Disorder
Diffuse C-Cell Hyperplasia
Ductal Breast Hyperplasia of Usual Type
Acute Myeloid Leukemia M5
Epithelial Neoplasm of Ovary of Borderline Malignancy
Epithelial Neoplasm of the Ovary of Borderline Malignancy
Epithelial Ovarian Neoplasm of Borderline Malignancy
Epithelial Ovarian Tumor of Borderline Malignancy
Epithelial Tumor of Ovary of Borderline Malignancy
Epithelial Tumor of the Ovary of Borderline Malignancy
Erosive Adenomatosis of Nipple
Erosive Adenomatosis of the Nipple
Erosive Nipple Adenomatosis
Erythema Multiforme Major
Esophageal Adenosquamous Carcinoma
Esophageal Undifferentiated Carcinoma
Factor VIII F8B
Familial Non-Polyposis Colon Cancer Type 1
Fibrosarcomatous Dermatofibrosarcoma Protuberans
Fibrous Papule
Follicular Variant Papillary Adenocarcinoma
Fredrickson Type V Lipidemia
Gastrointestinal Autonomic Nerve Tumor
Giant Cell Fibroblastoma
Giant Condyloma Acuminatum of Penis
Giant Condyloma Acuminatum of the Penis
Giant Condyloma Acuminatum
Giant Pigmented Nevus of Skin
Giant Pigmented Nevus of the Skin
Gigantiform Cementoma
Glandular Papilloma
Glial Neoplasm Spinal Cord
Glial Tumor of Spinal Cord
Grade 3 Follicular Lymphoma
Grade I Astrocytic Neoplasm
Grade I Astrocytic Tumor
Grade III Follicular Large Cell Lymphoma
Grade III Follicular Lymphoma
Granular Cast Formation
Great Vessel Cancer
HNPCC1
Hematopoietic Cancer
Hemophagocytic Syndrome
Hereditary Non-Polyposis Colon Cancer Type 1
Hypergranular Acute Promyelocytic Leukemia
Hyperimmunoglobulin E Syndrome
Iatrogenic Cancer
Adult Anaplastic (Malignant) Meningioma
Immunocytoma, Lymphoplasmacytic Type
Adult Anaplastic Meningioma
Immunoglobulin Deposition Disease
Impaired Renal Function
Inferior Vena Cava Occlusion
Inferolateral Myocardial Infarct
Intraepidermal Epithelioma of Jadassohn
Intraspinal Neoplasms
Intraspinal Neoplasm
Intraspinal Tumor
Kidney Cyst
Adult Malignant Meningioma
Leukemia Stem Cell
Lymphoplasmacytoid Lymphoma
Lynch 1 Syndrome
MART1
MLANA
Malignant Germ Cell Neoplasm
Malignant Germ Cell Tumor
Malignant Great Vessel Neoplasm
Malignant Great Vessel Tumor
American Cutaneous Leishmaniasis
Malignant Neoplasm of Germ Cell
Malignant Neoplasm of the Germ Cell
Malignant Tumor of Germ Cell
Malignant Tumor of the Germ Cell
Mammary adenocarcinoma
Mediastinal (Thymic) Large B-Cell Lymphoma
Mediastinal B-Cell Diffuse Large Cell Lymphoma
Melan-A Protein
Mesothelial Tumor
Metastases to Ovary
Metastasis to Ovary
Metastatic Cancer
Metastatic Malignant Neoplasm to the Ovary
Metastatic Malignant Neoplasm
Metastatic Malignant Tumor to the Ovary
Metastatic Neoplasm
Metastatic Tumor
Anaplastic Small Cell Carcinoma of Salivary Gland
Anaplastic Small Cell Carcinoma of the Salivary Gland
Monoclonal Immunoglobulin Deposition Disease
Myeloid Malignancy
Myeloid Neoplasm
Myeloid Tumor
Myocardial Disorder
Myxoid Fibrous Histiocytoma
Myxoid MFH
Nasal Sinus Cyst
Nasopharyngeal Carcinoma
Neoplasm of Placenta
Neoplasm of Spinal Canal and Spinal Cord
Neoplasm of Thymus
Neoplasm of the Placenta
Neoplasm of the Spinal Canal and Spinal Cord
Neoplasm of the Thymus
Neoplasms of Spinal Canal and Spinal Cord
Neoplasms of the Spinal Canal and Spinal Cord
Neoplastic Growth
Neuroectodermal Neoplasm
Neuroendocrine Carcinoma of Salivary Gland
Neuroendocrine Carcinoma of the Salivary Gland
Neutrophilic Leukemia
Non-Gonococcal Urethritis
Antigen LB39-AA
Antigen SK29-AA
Antihaemophilic Factor
Odontogenic Carcinoma
Odontogenic Carcinosarcoma
Ovarian Endometrioid Adenofibroma
Ovarian Metastasis
Ovarian Small Cell Carcinoma
PanIN
Pancreatic Intraepithelial Neoplasia
Papillary Carcinoma Follicular Variant
Arteriosclerotic Cardiovascular Disease
Paranasal Sinus Cyst
Partial Sight
Pediatric Cancer of Liver
Pediatric Cancer of the Liver
Pediatric Liver Cancer
Penile Buschke-Lowenstein Neoplasm
Penile Buschke-Lowenstein Tumor
Penile Giant Condyloma Acuminatum
Perihilar Extrahepatic Bile Duct Carcinoma
Placenta Neoplasms
Placenta Neoplasm
Placenta Tumors
Placenta Tumor
Placental Neoplasm
Placental Tumors
Placental Tumor
Plasmablastic Lymphoma
Atypical CML
Primary Mediastinal Large B-Cell Lymphoma
Primitive Neuroectodermal Neoplasm
Procoagulant Component
Prostate Cancer Stage D
B-Cell Diffuse Large Cell Lymphoma of Mediastinum
B-Cell Diffuse Large Cell Lymphoma of the Mediastinum
Refractory Carcinoma
Renal Cyst
Retroperitoneal Leiomyosarcoma
Salivary Gland Neuroendocrine Carcinoma
Secondary Cancer
Secondary Malignancy
Secondary Malignant Neoplasm
Secondary Neoplasm
Secondary Tumor
Selective IgA Immunodeficiency
Somatotropic Hormone
Spinal Canal Tumors
Spinal Canal and Spinal Cord Neoplasm
Spinal Canal and Spinal Cord Tumor
Spinal Chordomas
Spinal Chordoma
Spinal Column Chordoma
Spinal Cord Glial Neoplasms
Spinal Cord Glial Neoplasm
Spinal Cord Glial Tumors
Spinal Cord Glial Tumor
Spinal Tumors
Splenic Diffuse Large B-Cell Lymphoma
Splenic Follicular Lymphoma
Splenic Mantle Cell Lymphoma
Stage D Prostate Cancer
Bacterial Abscess
Bathing Trunk Nevus
Stage IVB Carcinoma of Lip
Stage IVB Carcinoma of the Lip
Subacute Granulocytic Leukemia
Subacute Myelogenous Leukemia
Subacute Myeloid Leukemia
Suppurative Granuloma
Therapy Related Malignant Tumor
Tooth Disorder
Toxoplasma Pneumonia
Tumor of Placenta
Tumor of Spinal Canal and Spinal Cord
Tumor of Thymus
Tumor of the Placenta
Tumor of the Spinal Canal and Spinal Cord
Tumor of the Thymus
Tumors of Ewing's Family
Tumors of the Ewing's Family
Type V Lipidemia
Typical Acute Promyelocytic Leukemia
UDH
Unicameral Bone Cyst
Ureter Disease
Ureteric Disease
Usual Ductal Breast Hyperplasia
Vaginal Hemorrhage
Venous Angioma
Vertebral Artery Syndrome
Viral Gastroenteritis
vWFAg
vWF
von Willebrand Factor Antigen
Blood Vessel Neoplasm
Borderline Epithelial Neoplasm of Ovary
Borderline Epithelial Neoplasm of the Ovary
Borderline Epithelial Tumor of Ovary
Borderline Epithelial Tumor of the Ovary
Borderline Ovarian Epithelial Neoplasm
Borst-Jadassohn Intraepidermal Carcinoma
Buschke-Lowenstein Neoplasm of Penis
Buschke-Lowenstein Neoplasm of the Penis
Buschke-Lowenstein Tumor of Penis
Buschke-Lowenstein Tumor of the Penis
Buschke-Lowenstein Tumor
CNS PNET
CNS Primitive Neuroectodermal Neoplasm
CNS Primitive Neuroectodermal Tumor
5q- Syndrome
Cancer of Prostate Stage D
Capillary Angioma
Carcinoma of Head and Neck
Carcinoma of the Head and Neck
Carcinoma of the Nasopharynx
Carotenosis Cutis
Central Nervous System PNET
Central Nervous System Primitive Neuroectodermal Neoplasm
Central Nervous System Primitive Neuroectodermal Tumor
Central Primitive Neuroectodermal Neoplasm
Central Primitive Neuroectodermal Tumor
Cervical Cancer Stage II
Childhood Cancer of Liver
Childhood Cancer of the Liver
Zoonotic Infection
Cancer of the Prostate Stage D
Iodine Uptake Alteration
Chelating Activity
BAY 54-9085
Benign Ovarian Endometrioid Tumor
Beta-ser-interferon
Borderline Ovarian Surface Epithelial-Stromal Tumor
CB/CC
COCA 1
Calcium DTPA
Calcium Pentetic Acid
Calcium-DTPA
Camptothecin-11
Chromosomal Rearrangement
5 Alpha-Reductase Inhibitor
Consensus Interferon
DHFR Inhibitor
DNA Methyltransferase Inhibitor
DNA Polymerase Inhibitor
Dephosphorylation
Diffuse Centroblastic-Centrocytic Lymphoma
Dihydrofolate Reductase Inhibitor
Enzyme Interaction
Ewing's Family of Tumors
Ewing's Family of Tumours
ADA Inhibitor
Free Radical Scavenging
HPV-16 E7 Peptide
Hematologic and Lymphocytic Disorder
High Grade Ovarian Endometrioid Stromal Sarcoma
I 131 HSA
APC 8024
APC8024
Interferon Beta-1B
Loss of Chromosome 11p
Loss of Chromosome 13q
MART-1 Antigen
MART-1 Tumor Antigen
MLANA Protein
Malignant Ovarian Steroid Cell Tumor
Melan A
Active Transporter Interaction
Melanoma Antigen Recognized by T-Cells 1
Microcystic Structures Present
Microinvasive Breast Carcinoma
Mistletoe Extract
MoAb Hu1D10
Monoclonal Antibody Anti-Avb3 Integrin
Monoclonal Antibody Hu1D10
Monosomy X
Murine Monoclonal Antibody 2B8
Myeleukon
NVB
Nitrogen Mustard Compound
OXT
Ordinary Intraductal Breast Hyperplasia
Osmotic Activity
Ovarian Adenoacanthoma
Ovarian Adenosquamous Carcinoma
Ovarian Clear Cell Adenocarcinofibroma
Ovarian Clear Cell Malignant Adenofibroma
Ovarian Endometrioid Adenocarcinoma with Squamous Differentiation
Ovarian Mucinous Adenocarcinofibroma
Ovarian Mucinous Malignant Adenofibroma
Ovarian Squamous Cell Carcinoma
Pentetic Acid Calcium
Prion Disease Pathway
Protein Methylation
Agonist
RH1
Recombinant Gonadorelin
Recombinant Human Growth Hormone
Recombinant Oncostatin M
Recombinant interferon beta-1b
Ribonucleotide Reductase Inhibitor
SERM-3
SERM3
Therapeutic GRH
Topical Anti-Infective Agent
Anti-infective Preparation
Transitional Cell Carcinoma of the Urinary Tract
Tyrosinase-Related Protein-2
Undifferentiated Ovarian Sarcoma
Urothelial Carcinoma
Vasopressin Antagonist
Vitamin A USP
Vulvar Apocrine Adenocarcinoma
Vulvar Basaloid Carcinoma
Vulvar Basaloid Squamous Cell Carcinoma
Vulvar Eccrine Adenocarcinoma
Vulvar Keratinizing Squamous Cell Carcinoma
Vulvar Leiomyosarcoma
Vulvar Liposarcoma
del(11p)
del(12)(p13)
del(12p13)
del(13q)
del(3p25)
mTOR Inhibitor
Adenosine Deaminase Inhibitor
Convulsions
Endoglycosidases
Enteritis, Granulomatous
Laroxyl
N(5)-Formyltetrahydrofolate
Rachitis
Self-Destructive Behavior
DF 118
FD&C violet no. 1
6R-L-erythro-5,6,7,8-tetrahydrobiopterin
Dyslalia
Amias
Esmeron
Apraxia, Articulatory
Arnold-Chiari Malformation, Type II
Therapy-Associated Cancer
Autosomal Recessive Juvenile Parkinson Disease
Blindness, Complete
Cacosmia
Sigmoid Cancer
Galactokinase Deficiency Disease
Encephalitis, Russian Spring-Summer
Hypoxic-Ischemic Encephalopathy
Rotational Nystagmus
Polycystic Kidney, Type 2 Autosomal Dominant Disease
aphobazole
caprylic acid, zinc salt
phenylacetic acid, sodium salt
Vergentan
Mummified Fetus
ibafloxacin
Erosive Duodenitis
Esmerone
dexanabinol
Benzetacil
Co-Translational Protein Modification
Sphincter of Oddi Dyskinesia
Amino Acid Modification, Co-Translational
Amino Acid Modification, Post-Translational
Iodoflex
Kenzen
Litican
dibasic calcium phosphate, anhydrous
Stenosis
Dermatophytosis of nail
Diaphoresis
Tinea unguium
Tinea of nail
Acute monocytic/monoblastic leukemia
Opthalmia neonatorum caused by Neisseria
Platelet count above reference range
Platelet count below reference range
Visual system finding
Desloratadine + pseudoephedrine sulfate
Vaginismus
Marcaine
calcium hydrogen phosphate
calcium phosphate, dibasic
Cotazym-S
glisentide
danaproid sodium
Abbott Brand of Bupivacaine Hydrochloride
Arthritis, Juvenile Idiopathic
Astra Brand of Prilocaine Hydrochloride
Cancer, Uterine Cervical
Cancers, Uterine Cervical
Cervical Cancer, Uterine
Cervical Cancers, Uterine
Cotazym S
Dysplasia, Multicystic Renal
Dysplasias, Multicystic Renal
Embden Meyerhof Parnas Pathway
Embden Meyerhof Pathway
Embden-Meyerhof Pathways
Embden-Meyerhof Pathway
Embden-Meyerhof-Parnas Pathway
Ergodryl Mono
Idiopathic Arthritis, Juvenile
Juvenile Idiopathic Arthritis
Minerval
Mono, Ergodryl
Multicystic Renal Dysplasias
Organon Brand 2 of Pancrelipase
Oxide, Ferriferrous
Pathway, Embden-Meyerhof-Parnas
Pathway, Embden-Meyerhof
Pathways, Embden-Meyerhof
Renal Dysplasia, Multicystic
Renal Dysplasias, Multicystic
Reproductive Sterility
Sterility, Reproductive
Usher Syndrome, Type I
Uterine Cervical Cancers
Multicystic Renal Dysplasia
Oxide, Ferrosoferric
Esoterica
atropine sulfate-diphenoxylate hydrochloride combination
cClB8 monoclonal antibody
monoclonal antibody CNTO-328
monoclonal antibody CNTO328
HIE syndrome
Hyperimmunoglobulin E syndrome
Keratinizing cyst of skin