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Gene–disease association summaries
Gene–Disease Browser
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| Gene |
Disease |
Score |
Actions |
|
TGFBR2
(HGNC:11773)
|
Loeys-Dietz syndrome 2
(MONDO_0012427)
|
Strong
|
|
|
TGFBR1
(HGNC:11772)
|
Loeys-Dietz syndrome 1
(MONDO_0012212)
|
Strong
|
|
|
TGFBR1
(HGNC:11772)
|
multiple self-healing squamous epithelioma
(MONDO_0007566)
|
Strong
|
|
|
TGFBI
(HGNC:11771)
|
granular corneal dystrophy type II
(MONDO_0011855)
|
Definitive
|
|
|
TGFBI
(HGNC:11771)
|
Reis-Bucklers corneal dystrophy
(MONDO_0012043)
|
Moderate
|
|
|
TGFBI
(HGNC:11771)
|
Thiel-Behnke corneal dystrophy
(MONDO_0011185)
|
Strong
|
|
|
TGFBI
(HGNC:11771)
|
lattice corneal dystrophy type I
(MONDO_0007380)
|
Strong
|
|
|
TGFBI
(HGNC:11771)
|
granular corneal dystrophy type I
(MONDO_0007377)
|
Strong
|
|
|
TGFBI
(HGNC:11771)
|
epithelial basement membrane dystrophy
(MONDO_0007375)
|
Limited
|
|
|
TGFB3
(HGNC:11769)
|
Loeys-Dietz syndrome
(MONDO_0018954)
|
Strong
|
|
|
TGFB2
(HGNC:11768)
|
Loeys-Dietz syndrome 4
(MONDO_0013897)
|
Moderate
|
|
|
TGFB3
(HGNC:11769)
|
arrhythmogenic right ventricular cardiomyopathy
(MONDO_0016587)
|
Refuted
|
|
|
TGFB3
(HGNC:11769)
|
Rienhoff syndrome
(MONDO_0014262)
|
Limited
|
|
|
TG
(HGNC:11764)
|
familial thyroid dyshormonogenesis
(MONDO_0010132)
|
Definitive
|
|
|
TGFB1
(HGNC:11766)
|
Camurati-Engelmann disease
(MONDO_0007542)
|
Definitive
|
|
|
TGFB1
(HGNC:11766)
|
cystic fibrosis
(MONDO_0009061)
|
Moderate
|
|
|
TFR2
(HGNC:11762)
|
hemochromatosis type 3
(MONDO_0011417)
|
Strong
|
|
|
TG
(HGNC:11764)
|
thyroid cancer
(MONDO_0002108)
|
Limited
|
|
|
TFG
(HGNC:11758)
|
hereditary spastic paraplegia 57
(MONDO_0014295)
|
Strong
|
|
|
TFAP2B
(HGNC:11743)
|
Char syndrome
(MONDO_0008209)
|
Definitive
|
|