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
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
Showing 4681–4700 of 6699