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
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
Showing 1681–1700 of 6699