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Diseases
Genes (959)
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TTPA
Familial Isolated Vitamin E Deficiency
FMR1
Disinhibition
Fragile X-Associated Tremor/ataxia Syndrome
Renpenning's Syndrome
Fg Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
GNAQ
Sturge–weber Syndrome
SLC17A5
Salla Disease
NGLY1
Ngly1 Deficiency
RASA1
Sturge–weber Syndrome
IL6
Uveitis
Fibrous Dysplasia Of Bone
Cholera
Familial Isolated Vitamin E Deficiency
Chronic Periodontitis
Subacromial Bursitis
TNF
Uveitis
Cholera
Familial Isolated Vitamin E Deficiency
Chronic Periodontitis
Renpenning's Syndrome
Salla Disease
Subacromial Bursitis
IL1B
Uveitis
Cholera
Chronic Periodontitis
Renpenning's Syndrome
Subacromial Bursitis
RBP3
Uveitis
IL17A
Uveitis
Cholera
Chronic Periodontitis
IL1A
Uveitis
Chronic Periodontitis
TNFSF11
Fibrous Dysplasia Of Bone
Chronic Periodontitis
SERPINF1
Uveitis
ALB
Uveitis
Cholera
Disinhibition
TLR4
Uveitis
Chronic Periodontitis
PRKACA
Fibrolamellar Hepatocellular Carcinoma
DNAJB1
Fibrolamellar Hepatocellular Carcinoma