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MYO5B

myosin VB

gene with protein productOMIM: 6065403 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)2
MYO5B-related progressive familial intrahepatic cholestasisORPHA:480491
→
Progressive familial intrahepatic cholestasis type 1ORPHA:79306
→
Disease-causing germline mutation(s) (loss of function) in1
Microvillus inclusion diseaseORPHA:2290
→
Данные: Orphadata (CC-BY-4.0)