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Diseases
Genes (1343)
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SH3TC2
Charcot-Marie-Tooth Neuropathy Type 4c
TRPC6
Focal Segmental Glomerulosclerosis
AR
Primary Ovarian Insufficiency
Partial Androgen Insensitivity Syndrome
MLH1
Synovial Sarcoma
Muir–torre Syndrome
KRT17
Pachyonychia Congenita
MSH2
Muir–torre Syndrome
COL4A1
Focal Segmental Glomerulosclerosis
Hemolytic Anemia
INF2
Focal Segmental Glomerulosclerosis
SSX1
Synovial Sarcoma
SSX2
Synovial Sarcoma
KRT16
Pachyonychia Congenita
PDGFRA
Chronic Myelomonocytic Leukemia
Hypereosinophilic Syndrome
Synovial Sarcoma
KDM6A
Focal Segmental Glomerulosclerosis
Chronic Myelomonocytic Leukemia
Hemolytic Anemia
SUFU
Joubert Syndrome 32
APOL1
African Trypanosomiasis
Focal Segmental Glomerulosclerosis
SS18
Synovial Sarcoma
G6PD
Hemolytic Anemia
AGT
Severe Acute Respiratory Syndrome
Focal Segmental Glomerulosclerosis
Primary Ovarian Insufficiency
MSH6
Muir–torre Syndrome
NOS2
African Trypanosomiasis
Focal Segmental Glomerulosclerosis