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MYPN

myopalladin

gene with protein productOMIM: 6085174 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)3
Familial isolated dilated cardiomyopathyORPHA:154
→
Cap myopathyORPHA:171881
→
Familial isolated restrictive cardiomyopathyORPHA:75249
→
Disease-causing germline mutation(s) (loss of function) in1
Childhood-onset nemaline myopathyORPHA:171439
→
Данные: Orphadata (CC-BY-4.0)