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Summary Literature (0)
MIM:161800 - CONGENITAL MYOPATHY 2A, TYPICAL, AUTOSOMAL DOMINANT; CMYP2A

Xenbase Genes: acta1, tpm3, tpm2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008070 - nemaline myopathy 3
MONDO:0015735 - severe congenital nemaline myopathy
MONDO:0015736 - intermediate nemaline myopathy
MONDO:0015737 - typical nemaline myopathy
MONDO:0015738 - childhood-onset nemaline myopathy
MONDO:0020342 - obsolete congenital myopathy with excess of thin filaments

Disease Ontology (DO):
DOID:0110927 - nemaline myopathy 3