Variant Synonymizer: Platform to identify mutations defined in different ways is available now!

VarSy

Over 2,000 gene–disease validation summaries are now available—no login required!

Browse Summaries

Stats

Total associations
6681
Unique genes
4239
Unique diseases
3297
Gene–disease association summaries
Back to Open Access Summaries

Gene–Disease Browser

Need updated, customized, evidence‑backed summaries? Get it from the leaders in AI‑powered, evidence‑backed summaries provider.
Contact us
Gene Disease Score Actions
FGF10
(HGNC:3666)
aplasia of lacrimal and salivary glands
(MONDO_0008397)
 Strong
FGF10
(HGNC:3666)
LADD syndrome
(MONDO_0007872)
 Strong
FGB
(HGNC:3662)
familial dysfibrinogenemia
(MONDO_0014452)
 Strong
FGB
(HGNC:3662)
congenital afibrinogenemia
(MONDO_0008737)
 Strong
FGA
(HGNC:3661)
AFib amyloidosis
(MONDO_0019733)
 Moderate
FGA
(HGNC:3661)
congenital fibrinogen deficiency
(MONDO_0018060)
 Strong
FGA
(HGNC:3661)
familial dysfibrinogenemia
(MONDO_0014452)
 Strong
FGA
(HGNC:3661)
congenital afibrinogenemia
(MONDO_0008737)
 Definitive
FBN1
(HGNC:3603)
isolated ectopia lentis
(MONDO_0015998)
 Strong
FBN1
(HGNC:3603)
familial thoracic aortic aneurysm and aortic dissection
(MONDO_0019625)
 Definitive
FBN1
(HGNC:3603)
progeroid and marfanoid aspect-lipodystrophy syndrome
(MONDO_0014831)
 Moderate
FBN1
(HGNC:3603)
Marfan syndrome
(MONDO_0007947)
 Definitive
FBN1
(HGNC:3603)
Acromicric dysplasia
(MONDO_0007055)
 Strong
FBN1
(HGNC:3603)
stiff skin syndrome
(MONDO_0008492)
 Moderate
FBN1
(HGNC:3603)
Shprintzen-Goldberg syndrome
(MONDO_0008426)
 Moderate
FBN1
(HGNC:3603)
geleophysic dysplasia
(MONDO_0000127)
 Strong
AIPL1
(HGNC:359)
Leber congenital amaurosis
(MONDO_0018998)
 Definitive
FBLN2
(HGNC:3601)
pulmonary arterial hypertension
(MONDO_0015924)
 Limited
AIPL1
(HGNC:359)
Leber congenital amaurosis 4
(MONDO_0011458)
 Strong
AIP
(HGNC:358)
pituitary gigantism
(MONDO_0020479)
 Strong
Showing 1681–1700 of 6681