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
FAS
(HGNC:11920)
autoimmune lymphoproliferative syndrome type 1
(MONDO_0011158)
 Definitive
CD40
(HGNC:11919)
hyper-IgM syndrome type 3
(MONDO_0011735)
 Strong
TNFRSF1A
(HGNC:11916)
autosomal dominant familial periodic fever
(MONDO_0007727)
 Definitive
TNFRSF11B
(HGNC:11909)
juvenile Paget disease
(MONDO_0009394)
 Definitive
TNFRSF11A
(HGNC:11908)
autosomal recessive osteopetrosis 7
(MONDO_0012859)
 Limited
TNFRSF11A
(HGNC:11908)
osteosarcoma
(MONDO_0009807)
 Refuted
ACO2
(HGNC:118)
optic atrophy 9
(MONDO_0014571)
 Moderate
TNFRSF11A
(HGNC:11908)
dysosteosclerosis
(MONDO_0009138)
 Moderate
TNFRSF11A
(HGNC:11908)
familial expansile osteolysis
(MONDO_0008275)
 Definitive
ACO2
(HGNC:118)
infantile cerebellar-retinal degeneration
(MONDO_0013802)
 Moderate
TNFAIP3
(HGNC:11896)
systemic lupus erythematosus
(MONDO_0007915)
 Strong
TMPO
(HGNC:11875)
dilated cardiomyopathy
(MONDO_0005021)
 Limited
TLK2
(HGNC:11842)
intellectual disability, autosomal dominant 57
(MONDO_0054837)
 Strong
TKT
(HGNC:11834)
transketolase deficiency
(MONDO_0014881)
 Moderate
TJP2
(HGNC:11828)
cholestasis, progressive familial intrahepatic, 4
(MONDO_0014381)
 Moderate
TK2
(HGNC:11831)
mitochondrial disease
(MONDO_0044970)
 Strong
NKX2-1
(HGNC:11825)
hereditary progressive chorea without dementia
(MONDO_0021011)
 Strong
NKX2-1
(HGNC:11825)
brain-lung-thyroid syndrome
(MONDO_0012593)
 Strong
TINF2
(HGNC:11824)
Hoyeraal-Hreidarsson syndrome
(MONDO_0018045)
 Moderate
TINF2
(HGNC:11824)
Revesz syndrome
(MONDO_0009990)
 Moderate
Showing 3821–3840 of 6699