Stats
Gene–disease association summaries
Gene–Disease Browser
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| Gene |
Disease |
Score |
Actions |
|
FGFR1
(HGNC:3688)
|
tooth agenesis
(MONDO_0005486)
|
Limited
|
|
|
FGFR1
(HGNC:3688)
|
Pfeiffer syndrome
(MONDO_0007043)
|
Strong
|
|
|
FGFR1
(HGNC:3688)
|
Jackson-Weiss syndrome
(MONDO_0007400)
|
Limited
|
|
|
FBN1
(HGNC:3603)
|
neonatal Marfan syndrome
(MONDO_0017309)
|
Definitive
|
|
|
FGA
(HGNC:3661)
|
thrombophilia
(MONDO_0002305)
|
Limited
|
|
|
AK2
(HGNC:362)
|
reticular dysgenesis
(MONDO_0009973)
|
Strong
|
|
|
FBN1
(HGNC:3603)
|
Weill-Marchesani syndrome
(MONDO_0018096)
|
Strong
|
|
|
FKTN
(HGNC:3622)
|
autosomal recessive limb-girdle muscular dystrophy type 2M
(MONDO_0012699)
|
Limited
|
|
|
FKTN
(HGNC:3622)
|
dilated cardiomyopathy 1X
(MONDO_0012704)
|
Moderate
|
|
|
FGF8
(HGNC:3686)
|
Kallmann syndrome
(MONDO_0018800)
|
Moderate
|
|
|
FGF8
(HGNC:3686)
|
hypogonadotropic hypogonadism
(MONDO_0018555)
|
Strong
|
|
|
FGF8
(HGNC:3686)
|
holoprosencephaly
(MONDO_0016296)
|
Moderate
|
|
|
FGF3
(HGNC:3681)
|
deafness with labyrinthine aplasia, microtia, and microdontia
(MONDO_0012541)
|
Strong
|
|
|
FGF17
(HGNC:3673)
|
Kallmann syndrome
(MONDO_0018800)
|
Limited
|
|
|
FGF16
(HGNC:3672)
|
syndactyly type 8
(MONDO_0010669)
|
Moderate
|
|
|
FGF12
(HGNC:3668)
|
developmental and epileptic encephalopathy
(MONDO_0100062)
|
Strong
|
|
|
FGF10
(HGNC:3666)
|
craniosynostosis
(MONDO_0015469)
|
Limited
|
|
|
FGA
(HGNC:3661)
|
familial visceral amyloidosis
(MONDO_0007099)
|
Limited
|
|
|
FGF10
(HGNC:3666)
|
aplasia of lacrimal and salivary glands
(MONDO_0008397)
|
Strong
|
|
|
FGF10
(HGNC:3666)
|
LADD syndrome
(MONDO_0007872)
|
Strong
|
|