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Diseases
Genes (1204)
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MYO5B
Microvillus Inclusion Disease
SMAD4
Juvenile Polyposis Syndrome
Adenoid Cystic Carcinoma
BMPR1A
Juvenile Polyposis Syndrome
F12
Factor Xii Deficiency
SLC12A6
Andermann Syndrome
FMR1
Fragile X-Associated Tremor/ataxia Syndrome
PTEN
Insulin Resistance
Salmonellosis
Membranoproliferative Glomerulonephritis
Kyphosis
Juvenile Polyposis Syndrome
Adenoid Cystic Carcinoma
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
CTNNB1
Fibrous Dysplasia Of Bone
Craniopharyngioma
Juvenile Polyposis Syndrome
Adenoid Cystic Carcinoma
Germinoma
ENG
Foix-Alajouanine Syndrome
Juvenile Polyposis Syndrome
MC2R
Familial Glucocorticoid Deficiency
BRAF
Craniopharyngioma
Factor Xii Deficiency
CFH
Salmonellosis
Membranoproliferative Glomerulonephritis
Factor Xii Deficiency
ALB
Membranoproliferative Glomerulonephritis
Melancholia
Craniopharyngioma
SOD1
Melancholia
Fragile X-Associated Tremor/ataxia Syndrome
Turner Syndrome
PON1
Membranoproliferative Glomerulonephritis
Melancholia
TP53
Disseminated Superficial Actinic Porokeratosis
Turner Syndrome
Juvenile Polyposis Syndrome
Adenoid Cystic Carcinoma
Germinoma
SLC6A4
Melancholia
PIK3CA
Insulin Resistance
Membranoproliferative Glomerulonephritis
Kyphosis
Juvenile Polyposis Syndrome
Adenoid Cystic Carcinoma
STX3
Microvillus Inclusion Disease