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Summary Literature (0)
MIM:609284 - CONGENITAL MYOPATHY 4B, AUTOSOMAL RECESSIVE; CMYP4B

Xenbase Genes: tpm3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012239 - congenital myopathy 4B, autosomal recessive
MONDO:0015736 - intermediate nemaline myopathy
MONDO:0015738 - childhood-onset nemaline myopathy
MONDO:0015753 - cap myopathy

Disease Ontology (DO):
DOID:0110926 - nemaline myopathy 1