Stats

Total associations
6699
Unique genes
4252
Unique diseases
3300
Gene–disease association summaries
Back to Open Access Summaries

Gene–Disease Browser

Need updated, customized, evidence‑backed summaries? Get it from the leaders in AI‑powered, evidence‑backed summaries provider.
Contact us
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
Showing 3861–3880 of 6699