congenital myopathy

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Echinobase

Summary

Literature (0)

DOID:0081337 - congenital myopathy

Disease Ontology Definition:A myopathy that is characterized by hypotonia and weakness, usually present from birth.

Synonyms:

Echinobase 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

: selenon

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

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

Parent(s): myopathy (is_a)