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Gene–disease association summaries
Gene–Disease Browser
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| Gene |
Disease |
Score |
Actions |
|
FGFR2
(HGNC:3689)
|
LADD syndrome
(MONDO_0007872)
|
Moderate
|
|
|
FGFR2
(HGNC:3689)
|
Pfeiffer syndrome type 2
(MONDO_0019660)
|
Strong
|
|
|
FGFR2
(HGNC:3689)
|
Antley-Bixler syndrome
(MONDO_0008803)
|
Moderate
|
|
|
FGFR2
(HGNC:3689)
|
Crouzon syndrome
(MONDO_0007405)
|
Definitive
|
|
|
FGFR2
(HGNC:3689)
|
Pfeiffer syndrome
(MONDO_0007043)
|
Definitive
|
|
|
FGFR2
(HGNC:3689)
|
Beare-Stevenson cutis gyrata syndrome
(MONDO_0007412)
|
Strong
|
|
|
FGFR2
(HGNC:3689)
|
Apert syndrome
(MONDO_0007041)
|
Definitive
|
|
|
FGFR2
(HGNC:3689)
|
Saethre-Chotzen syndrome
(MONDO_0007042)
|
Limited
|
|
|
FGFR1
(HGNC:3688)
|
hypogonadotropic hypogonadism
(MONDO_0018555)
|
Strong
|
|
|
FGFR1
(HGNC:3688)
|
Kallmann syndrome
(MONDO_0018800)
|
Strong
|
|
|
FGFR1
(HGNC:3688)
|
Hartsfield-Bixler-Demyer syndrome
(MONDO_0014196)
|
Strong
|
|
|
FGFR1
(HGNC:3688)
|
holoprosencephaly
(MONDO_0016296)
|
Moderate
|
|
|
FGFR1
(HGNC:3688)
|
septooptic dysplasia
(MONDO_0008428)
|
Limited
|
|
|
FGFR1
(HGNC:3688)
|
encephalocraniocutaneous lipomatosis
(MONDO_0013074)
|
Moderate
|
|
|
AIRE
(HGNC:360)
|
autoimmune polyendocrine syndrome type 1
(MONDO_0009411)
|
Definitive
|
|
|
FCGR3B
(HGNC:3620)
|
systemic lupus erythematosus
(MONDO_0007915)
|
Moderate
|
|
|
FGF9
(HGNC:3687)
|
multiple synostoses syndrome
(MONDO_0017923)
|
Strong
|
|
|
FGFR1
(HGNC:3688)
|
osteoglophonic dwarfism
(MONDO_0008150)
|
Moderate
|
|
|
FCGR2B
(HGNC:3618)
|
systemic lupus erythematosus
(MONDO_0007915)
|
Moderate
|
|
|
FKTN
(HGNC:3622)
|
muscle-eye-brain disease
(MONDO_0018939)
|
Limited
|
|