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Diseases
Genes (1575)
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SSX1
Synovial Sarcoma
SSX2
Synovial Sarcoma
SLC4A1
Hemolytic Anemia
Cryohydrocytosis
COL4A1
Focal Segmental Glomerulosclerosis
Hemolytic Anemia
Intracerebral Hemorrhage
SS18
Synovial Sarcoma
DAB1
Spinocerebellar Ataxia Type 37
Spinocerebellar Ataxia 37
BCL2
Synovial Sarcoma
Focal Segmental Glomerulosclerosis
B-Cell Prolymphocytic Leukemia
Primary Ovarian Insufficiency
Cryohydrocytosis
Intracerebral Hemorrhage
TRPC6
Focal Segmental Glomerulosclerosis
SOX10
Yemenite Deaf-Blind Hypopigmentation Syndrome
Synovial Sarcoma
Delayed Puberty
ACE
Synovial Sarcoma
Severe Acute Respiratory Syndrome
Focal Segmental Glomerulosclerosis
Primary Ovarian Insufficiency
Intracerebral Hemorrhage
ATXN2
Spinocerebellar Ataxia Type 2
SLC24A1
Intracerebral Hemorrhage
Night Blindness, Congenital Stationary, Type 1b
SCN5A
Ventricular Fibrillation, Paroxysmal Familial, 2
SUFU
Joubert Syndrome 32
Intracerebral Hemorrhage
INF2
Focal Segmental Glomerulosclerosis
RHO
Night Blindness, Congenital Stationary, Type 1b
GRM6
Night Blindness, Congenital Stationary, Type 1b
TRPM1
Night Blindness, Congenital Stationary, Type 1b
HMOX1
Focal Segmental Glomerulosclerosis
Hemolytic Anemia
Primary Ovarian Insufficiency
Intracerebral Hemorrhage
GNAT1
Night Blindness, Congenital Stationary, Type 1b