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Summary Literature (0)
MIM:605355 - NEMALINE MYOPATHY 5A, SEVERE INFANTILE; NEM5A

Xenbase Genes: tnnt1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011539 - nemaline myopathy 5

Disease Ontology (DO):
DOID:0110936 - nemaline myopathy 5A