← Назад
🧬

TGFBR1

transforming growth factor beta receptor 1

gene with protein productOMIM: 1901814 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)3
Marfan syndrome type 2ORPHA:284973
→
Loeys-Dietz syndromeORPHA:60030
→
Familial thoracic aortic aneurysm and aortic dissectionORPHA:91387
→
Disease-causing germline mutation(s) (loss of function) in1
Multiple self-healing squamous epitheliomaORPHA:65748
→
Данные: Orphadata (CC-BY-4.0)