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Diseases
Genes (1615)
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SH3TC2
Charcot-Marie-Tooth Neuropathy Type 4c
UGT1A1
Gilbert's Syndrome
SOX10
Yemenite Deaf-Blind Hypopigmentation Syndrome
Charcot-Marie-Tooth Neuropathy Type 4c
TNF
Severe Acute Respiratory Syndrome
African Trypanosomiasis
Primary Ovarian Insufficiency
Salmonellosis
Seborrhoeic Dermatitis
Cardiomyopathy
Candidiasis
Chronic Myelomonocytic Leukemia
PLN
Cardiomyopathy
TNNT2
Cardiomyopathy
MYBPC3
Cardiomyopathy
DMD
Cardiomyopathy
TNNI3
Cardiomyopathy
DES
Cardiomyopathy
SGCD
Cardiomyopathy
KDM6A
Chronic Myelomonocytic Leukemia
CRYAB
Cardiomyopathy
TAZ
Cardiomyopathy
EMD
Cardiomyopathy
MYH7
Cardiomyopathy
PRKAG2
Cardiomyopathy
DSP
Cardiomyopathy
PKP2
Cardiomyopathy
TTN
Cardiomyopathy