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Diseases
Genes (1128)
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MYO5B
Microvillus Inclusion Disease
POLG
Balo Concentric Sclerosis
SLC12A6
Andermann Syndrome
FMR1
Fragile X-Associated Tremor/ataxia Syndrome
HLA-DRB1
Night Sweats
Thalassemia
Sarcoidosis, Susceptibility To, 1
SLC17A5
Salla Disease
PMM2
Pmm2 Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
BTNL2
Sarcoidosis, Susceptibility To, 1
TP53
Disseminated Superficial Actinic Porokeratosis
Fibrolamellar Hepatocellular Carcinoma
Adenoid Cystic Carcinoma
STX3
Microvillus Inclusion Disease
ANXA11
Sarcoidosis, Susceptibility To, 1
PIK3CA
Salla Disease
Adenoid Cystic Carcinoma
Sarcoidosis, Susceptibility To, 1
NOTCH1
Adenoid Cystic Carcinoma
PTEN
Thrombophlebitis
Adenoid Cystic Carcinoma
Lumbar Disc Disease
MYB
Thalassemia
Adenoid Cystic Carcinoma
MRAP
Familial Glucocorticoid Deficiency
PRKACA
Fibrolamellar Hepatocellular Carcinoma
DNAJB1
Fibrolamellar Hepatocellular Carcinoma