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Summary Literature (0)
MIM:609285 - NEMALINE MYOPATHY 4; NEM4

Xenbase Genes: tpm2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012240 - congenital myopathy 23
MONDO:0015737 - typical nemaline myopathy
MONDO:0015738 - childhood-onset nemaline myopathy
MONDO:0015753 - cap myopathy

Disease Ontology (DO):
DOID:0110932 - nemaline myopathy 4