|
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)
|
Strong
|
|
|
FKTN
(HGNC:3622)
|
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4
(MONDO_0009678)
|
Strong
|
|
|
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
|
|
|
EYA1
(HGNC:3519)
|
branchio-oto-renal syndrome
(MONDO_0007029)
|
Definitive
|
|
|
EXT2
(HGNC:3513)
|
hereditary multiple osteochondromas
(MONDO_0005508)
|
Definitive
|
|