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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
FGF23
(HGNC:3680)
familial tumoral calcinosis
(MONDO_0018891)
 Strong
FGG
(HGNC:3694)
familial dysfibrinogenemia
(MONDO_0014452)
 Strong
FGF23
(HGNC:3680)
familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
(MONDO_0100251)
 Strong
FGF23
(HGNC:3680)
autosomal dominant hypophosphatemic rickets
(MONDO_0008660)
 Definitive
FGF14
(HGNC:3671)
spinocerebellar ataxia type 27
(MONDO_0012247)
 Strong
FGD1
(HGNC:3663)
Aarskog-Scott syndrome, X-linked
(MONDO_0010589)
 Definitive
FECH
(HGNC:3647)
erythropoietic protoporphyria
(MONDO_0001676)
 Definitive
FKTN
(HGNC:3622)
muscular dystrophy-dystroglycanopathy, type A
(MONDO_0000171)
 Definitive
FKTN
(HGNC:3622)
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4
(MONDO_0009678)
 Definitive
FBP1
(HGNC:3606)
fructose-1,6-bisphosphatase deficiency
(MONDO_0009251)
 Definitive
FBN2
(HGNC:3604)
congenital contractural arachnodactyly
(MONDO_0007363)
 Definitive
F9
(HGNC:3551)
hemophilia B
(MONDO_0010604)
 Definitive
F7
(HGNC:3544)
congenital factor VII deficiency
(MONDO_0009211)
 Definitive
F7
(HGNC:3544)
factor VII deficiency
(MONDO_0002244)
 Definitive
F13A1
(HGNC:3531)
factor XIII deficiency
(MONDO_0002241)
 Definitive
F13A1
(HGNC:3531)
congenital factor XIII deficiency
(MONDO_0018029)
 Definitive
F12
(HGNC:3530)
hereditary angioedema
(MONDO_0019623)
 Strong
F10
(HGNC:3528)
congenital factor X deficiency
(MONDO_0009212)
 Definitive
F10
(HGNC:3528)
factor X deficiency
(MONDO_0002247)
 Definitive
EYA1
(HGNC:3519)
branchiootic syndrome
(MONDO_0018878)
 Strong
Showing 4681–4700 of 6681