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Echinobase
Summary Literature (0)
DOID:0080102 - congenital myopathy 4A

Disease Ontology Definition:A congenital myopathy that is characterized by skeletal muscle weakness, particularly in the muscles of the shoulders, upper arms, hips, and thighs.

Synonyms: CFTD, congenital fiber-type disproportion

Echinobase Genes : selenon


MIM:
MIM:255310 - myopathy, congenital, with fiber-type disproportion; cftd

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), congenital myopathy (is_a), physical disorder (is_a)