congenital structural myopathy

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Echinobase

Summary

Literature (0)

DOID:422 - congenital structural myopathy

Disease Ontology Definition:A myopathy that is characterized by hypotonia, muscle weakness, and delayed development of motor skills.

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

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

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

Parent(s): congenital myopathy (is_a), myopathy (is_a), physical disorder (is_a)