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Summary Literature (0)
DOID:0110931 - nemaline myopathy 10

Disease Ontology Definition: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: NEM10, congenital myopathy 10,

Xenbase Genes : lmod3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014513 - nemaline myopathy 10


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), nemaline myopathy (is_a)