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 |
|
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
|
|