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
TF
(HGNC:11740)
atransferrinemia
(MONDO_0008846)
 Moderate
TERT
(HGNC:11730)
acute myeloid leukemia
(MONDO_0018874)
 Moderate
TERT
(HGNC:11730)
Hoyeraal-Hreidarsson syndrome
(MONDO_0018045)
 Strong
TEK
(HGNC:11724)
primary congenital glaucoma
(MONDO_0000365)
 Strong
TERT
(HGNC:11730)
dyskeratosis congenita
(MONDO_0015780)
 Definitive
TECTA
(HGNC:11720)
autosomal dominant nonsyndromic hearing loss
(MONDO_0019587)
 Definitive
TECTA
(HGNC:11720)
autosomal recessive nonsyndromic hearing loss 21
(MONDO_0011351)
 Limited
TEAD1
(HGNC:11714)
Aicardi syndrome
(MONDO_0010568)
 Limited
TDO2
(HGNC:11708)
familial hypertryptophanemia
(MONDO_0010907)
 Limited
ZEB1
(HGNC:11642)
posterior polymorphous corneal dystrophy
(MONDO_0020364)
 Strong
ZEB1
(HGNC:11642)
Fuchs' endothelial dystrophy
(MONDO_0005321)
 Disputed
ZEB1
(HGNC:11642)
posterior polymorphous corneal dystrophy 3
(MONDO_0012200)
 Strong
TCF4
(HGNC:11634)
Pitt-Hopkins syndrome
(MONDO_0012589)
 Definitive
TCF4
(HGNC:11634)
Fuchs' endothelial dystrophy
(MONDO_0005321)
 Strong
TCF4
(HGNC:11634)
autism spectrum disorder
(MONDO_0005258)
 Moderate
TCF4
(HGNC:11634)
intellectual disability
(MONDO_0001071)
 Strong
HNF1B
(HGNC:11630)
permanent neonatal diabetes mellitus
(MONDO_0100164)
 Limited
HNF1B
(HGNC:11630)
unilateral multicystic dysplastic kidney
(MONDO_0019981)
 Limited
HNF1A
(HGNC:11621)
maturity-onset diabetes of the young
(MONDO_0018911)
 Definitive
TCF12
(HGNC:11623)
Kallmann syndrome
(MONDO_0018800)
 Moderate
Showing 3881–3900 of 6699