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
XPA
(HGNC:12814)
xeroderma pigmentosum group A
(MONDO_0010210)
 Definitive
WWOX
(HGNC:12799)
developmental and epileptic encephalopathy
(MONDO_0100062)
 Strong
WWOX
(HGNC:12799)
developmental and epileptic encephalopathy, 28
(MONDO_0014533)
 Strong
WT1
(HGNC:12796)
Denys-Drash syndrome
(MONDO_0008682)
 Definitive
WWOX
(HGNC:12799)
autosomal recessive spinocerebellar ataxia 12
(MONDO_0013687)
 Moderate
WT1
(HGNC:12796)
Frasier syndrome
(MONDO_0007635)
 Definitive
WRN
(HGNC:12791)
Werner syndrome
(MONDO_0010196)
 Definitive
WRN
(HGNC:12791)
osteosarcoma
(MONDO_0009807)
 Limited
WNT7A
(HGNC:12786)
Fuhrmann syndrome
(MONDO_0009232)
 Moderate
WNT7A
(HGNC:12786)
phocomelia, Schinzel type
(MONDO_0010164)
 Moderate
WNT5A
(HGNC:12784)
autosomal dominant Robinow syndrome
(MONDO_0008389)
 Strong
WNT10B
(HGNC:12775)
split hand-foot malformation 6
(MONDO_0009157)
 Moderate
WNT10B
(HGNC:12775)
tooth agenesis
(MONDO_0005486)
 Moderate
WNT1
(HGNC:12774)
osteogenesis imperfecta type 15
(MONDO_0014086)
 Strong
NSD2
(HGNC:12766)
Rauch-Steindl syndrome
(MONDO_0859219)
 Strong
WFS1
(HGNC:12762)
Wolfram syndrome
(MONDO_0018105)
 Definitive
FOXN1
(HGNC:12765)
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
(MONDO_0011132)
 Strong
WFS1
(HGNC:12762)
Wolfram-like syndrome
(MONDO_0013673)
 Strong
WFS1
(HGNC:12762)
Wolfram syndrome 1
(MONDO_0009101)
 Definitive
WFS1
(HGNC:12762)
type 2 diabetes mellitus
(MONDO_0005148)
 Strong
Showing 3621–3640 of 6699