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Stats

Total associations
6681
Unique genes
4239
Unique diseases
3297
Gene–disease association summaries
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Gene–Disease Browser

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Gene Disease Score Actions
UTP4
(HGNC:1983)
hereditary North American Indian childhood cirrhosis
(MONDO_0011497)
 Strong
TSSK4
(HGNC:19825)
male infertility
(MONDO_0005372)
 Limited
CIDEB
(HGNC:1977)
metabolic dysfunction-associated steatotic liver disease
(MONDO_0013209)
 Moderate
CIDEB
(HGNC:1977)
cirrhosis of liver
(MONDO_0005155)
 Disputed
CANT1
(HGNC:19721)
Desbuquois dysplasia
(MONDO_0015426)
 Definitive
CIDEA
(HGNC:1976)
obesity disorder
(MONDO_0011122)
 Limited
FNBP4
(HGNC:19752)
microphthalmia with limb anomalies
(MONDO_0008800)
 Limited
STXBP4
(HGNC:19694)
breast cancer
(MONDO_0007254)
 Limited
FGFBP1
(HGNC:19695)
hypertensive disorder
(MONDO_0005044)
 Limited
RD3
(HGNC:19689)
Leber congenital amaurosis
(MONDO_0018998)
 Strong
GPBAR1
(HGNC:19680)
primary sclerosing cholangitis
(MONDO_0013433)
 Limited
UHMK1
(HGNC:19683)
schizophrenia
(MONDO_0005090)
 Limited
CHRM5
(HGNC:1954)
cauda equina syndrome with neurogenic bladder
(MONDO_0020767)
 Limited
GPBAR1
(HGNC:19680)
ulcerative colitis
(MONDO_0005101)
 Limited
TNNI3K
(HGNC:19661)
dilated cardiomyopathy
(MONDO_0005021)
 Moderate
CHN1
(HGNC:1943)
Duane retraction syndrome
(MONDO_0007473)
 Strong
CHRM5
(HGNC:1954)
congenital anomaly of kidney and urinary tract
(MONDO_0019719)
 Limited
ALG12
(HGNC:19358)
ALG12-congenital disorder of glycosylation
(MONDO_0011783)
 Strong
DPY19L2
(HGNC:19414)
spermatogenic failure 6
(MONDO_0007060)
 Definitive
ALG12
(HGNC:19358)
congenital disorder of glycosylation
(MONDO_0015286)
 Strong
Showing 6121–6140 of 6681