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Summary Literature (0)
DOID:0110933 - nemaline myopathy 11

Disease Ontology Definition:A nemaline myopathy characterized by onset of slowly progressive muscle weakness in the first decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the MYPN gene on chromosome 10q21.

Synonyms: NEM11, nemaline myopathy 11, autosomal recessive

Xenbase Genes : mypn

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0015023 - MYPN-related myopathy


Other Model Organisms: Alliance, 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)