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LMOD3

leiomodin 3

gene with protein productOMIM: 6161122 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Disease-causing germline mutation(s) (loss of function) in2
Severe congenital nemaline myopathyORPHA:171430
→
Typical nemaline myopathyORPHA:171436
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Данные: Orphadata (CC-BY-4.0)