Stats
Gene–disease association summaries
Gene–Disease Browser
Need updated, customized, evidence‑backed summaries?
Get it from the leaders in AI‑powered, evidence‑backed summaries provider.
| Gene |
Disease |
Score |
Actions |
|
ALAS2
(HGNC:397)
|
X-linked sideroblastic anemia 1
(MONDO_0020721)
|
Definitive
|
|
|
ALAS2
(HGNC:397)
|
X-linked erythropoietic protoporphyria
(MONDO_0010420)
|
Definitive
|
|
|
FSHR
(HGNC:3969)
|
premature menopause
(MONDO_0001119)
|
Moderate
|
|
|
FXN
(HGNC:3951)
|
Friedreich ataxia
(MONDO_0100339)
|
Definitive
|
|
|
FOXG1
(HGNC:3811)
|
Rett syndrome, congenital variant
(MONDO_0013270)
|
Definitive
|
|
|
FOXF1
(HGNC:3809)
|
alveolar capillary dysplasia with misalignment of pulmonary veins
(MONDO_0009934)
|
Definitive
|
|
|
FOXG1
(HGNC:3811)
|
Rett syndrome
(MONDO_0010726)
|
Strong
|
|
|
FOXE1
(HGNC:3806)
|
congenital hypothyroidism
(MONDO_0018612)
|
Strong
|
|
|
FOXC2
(HGNC:3801)
|
lymphedema-distichiasis syndrome
(MONDO_0007922)
|
Definitive
|
|
|
FN1
(HGNC:3778)
|
fibronectin glomerulopathy
(MONDO_0007671)
|
Strong
|
|
|
FOLR1
(HGNC:3791)
|
cerebral folate deficiency
(MONDO_0100034)
|
Strong
|
|
|
FMO3
(HGNC:3771)
|
trimethylaminuria
(MONDO_0011182)
|
Definitive
|
|
|
FLT4
(HGNC:3767)
|
lymphatic malformation 1
(MONDO_0007919)
|
Definitive
|
|
|
FHL1
(HGNC:3702)
|
reducing body myopathy
(MONDO_0019948)
|
Definitive
|
|
|
FLI1
(HGNC:3749)
|
Ewing sarcoma
(MONDO_0012817)
|
Moderate
|
|
|
FGG
(HGNC:3694)
|
congenital afibrinogenemia
(MONDO_0008737)
|
Strong
|
|
|
FHL1
(HGNC:3702)
|
Emery-Dreifuss muscular dystrophy
(MONDO_0016830)
|
Strong
|
|
|
FHL1
(HGNC:3702)
|
hypertrophic cardiomyopathy
(MONDO_0005045)
|
Moderate
|
|
|
FGF23
(HGNC:3680)
|
familial tumoral calcinosis
(MONDO_0018891)
|
Strong
|
|
|
FGG
(HGNC:3694)
|
familial dysfibrinogenemia
(MONDO_0014452)
|
Definitive
|
|