distal myopathy 1

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Summary

Literature (0)

DOID:0070197 - distal myopathy 1

Disease Ontology Definition:A distal myopathy that is characterized by autosomal dominant inheritance that has_material_basis_in mutation in the MYH7 gene on chromosome 14q11.2.

Synonyms: Distal myopathy type 1, Gowers disease, Laing distal myopathy, Laing early-onset distal myopathy, MPD1

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: myh7l

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), distal myopathy (is_a)