Stats

Total associations
6699
Unique genes
4252
Unique diseases
3300
Gene–disease association summaries
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Gene–Disease Browser

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Gene Disease Score Actions
OTUD4
(HGNC:24949)
prostate cancer
(MONDO_0008315)
 Limited
GSX2
(HGNC:24959)
diencephalic-mesencephalic junction dysplasia
(MONDO_0017868)
 Limited
ZC4H2
(HGNC:24931)
Wieacker-Wolff syndrome
(MONDO_0010758)
 Strong
STBD1
(HGNC:24854)
Parkinson disease
(MONDO_0005180)
 Limited
LARP7
(HGNC:24912)
microcephalic primordial dwarfism, Alazami type
(MONDO_0014031)
 Strong
OTUD4
(HGNC:24949)
breast cancer
(MONDO_0007254)
 Limited
CCDC47
(HGNC:24856)
trichohepatoneurodevelopmental syndrome
(MONDO_0032645)
 Strong
PNPLA4
(HGNC:24887)
epilepsy
(MONDO_0005027)
 Limited
YIPF5
(HGNC:24877)
neonatal diabetes mellitus
(MONDO_0016391)
 Strong
MOGS
(HGNC:24862)
congenital disorder of glycosylation
(MONDO_0015286)
 Strong
CCDC91
(HGNC:24855)
breast cancer
(MONDO_0007254)
 Limited
CEP104
(HGNC:24866)
Joubert syndrome
(MONDO_0018772)
 Moderate
ENHO
(HGNC:24838)
type 2 diabetes mellitus
(MONDO_0005148)
 Limited
FN3K
(HGNC:24822)
diabetes mellitus
(MONDO_0005015)
 Limited
CIBAR2
(HGNC:24781)
ulcerative colitis
(MONDO_0005101)
 Disputed
VWA2
(HGNC:24709)
congenital anomaly of kidney and urinary tract
(MONDO_0019719)
 Limited
GPRASP1
(HGNC:24834)
arteriovenous hemangioma/malformation
(MONDO_0001256)
 Limited
LONRF2
(HGNC:24788)
colorectal cancer
(MONDO_0005575)
 Limited
KLRG2
(HGNC:24778)
prostate cancer
(MONDO_0008315)
 Limited
PTCD3
(HGNC:24717)
Leigh syndrome
(MONDO_0009723)
 Strong
Showing 5881–5900 of 6699