FGFR2
fibroblast growth factor receptor 2
Ассоциированные заболевания
Герминативная мутация (причина)6
Familial scaphocephaly syndrome, McGillivray typeORPHA:168624
→Jackson-Weiss syndromeORPHA:1540
→Cutis gyrata-acanthosis nigricans-craniosynostosis syndromeORPHA:1555
→Lacrimoauriculodentodigital syndromeORPHA:2363
→FGFR2-related bent bone dysplasiaORPHA:313855
→Antley-Bixler syndrome without genital anomaly or disorder of steroidogenesisORPHA:596008
→Disease-causing germline mutation(s) (gain of function) in5
Ген-кандидат1