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Disease Ontology Term: nemaline myopathy 10

DO ID
DOID:0110931
Description
A nemaline myopathy characterized by early-onset generalized muscle weakness and hypotonia with respiratory insufficiency and feeding difficulties that has_material_basis_in homozygous or compound heterozygous mutation in the LMOD3 gene on chromosome 3p14.
Synonyms
congenital myopathy 10, NEM10
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