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MIM:616165 - NEMALINE MYOPATHY 10; NEM10
Xenbase Genes: lmod3
Human Disease Resource: MIM
MONDO:0014513 - nemaline myopathy 10 |
MONDO:0015735 - severe congenital nemaline myopathy |
MONDO:0015737 - typical nemaline myopathy |
DOID:0110931 - nemaline myopathy 10 |