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Diseases
Genes (1721)
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BCL2
Synovial Sarcoma
Focal Segmental Glomerulosclerosis
B-Cell Prolymphocytic Leukemia
Primary Ovarian Insufficiency
Intracerebral Hemorrhage
Edwards Syndrome
Follicular Lymphoma
COL4A1
Focal Segmental Glomerulosclerosis
Hemolytic Anemia
Intracerebral Hemorrhage
TRPC6
Focal Segmental Glomerulosclerosis
SSX1
Synovial Sarcoma
SSX2
Synovial Sarcoma
SUFU
Joubert Syndrome 32
Intracerebral Hemorrhage
SH3TC2
Charcot-Marie-Tooth Neuropathy Type 4c
WT1
Xy Gonadal Dysgenesis
Focal Segmental Glomerulosclerosis
Primary Ovarian Insufficiency
PMP22
Charcot-Marie-Tooth Neuropathy Type 4c
Monosomy
Hereditary Neuropathy With Liability To Pressure Palsy
SS18
Synovial Sarcoma
SLC39A4
Acrodermatitis Enteropathica
INF2
Focal Segmental Glomerulosclerosis
NR5A1
Xy Gonadal Dysgenesis
Primary Ovarian Insufficiency
NSD2
Wolf–hirschhorn Syndrome
Microdeletion Syndrome
HMOX1
Focal Segmental Glomerulosclerosis
Hemolytic Anemia
Autoimmune Hemolytic Anemia
Primary Ovarian Insufficiency
Intracerebral Hemorrhage
ACE
Synovial Sarcoma
Focal Segmental Glomerulosclerosis
Primary Ovarian Insufficiency
Intracerebral Hemorrhage
Severe Acute Respiratory Syndrome
CYP11B1
Hyperaldosteronism, Familial, Type I
AGT
Focal Segmental Glomerulosclerosis
Primary Ovarian Insufficiency
Severe Acute Respiratory Syndrome
Hyperaldosteronism, Familial, Type I
SPP1
Focal Segmental Glomerulosclerosis
Intracerebral Hemorrhage
G6PD
Hemolytic Anemia