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Summary Literature (0)
DOID:9884 - muscular dystrophy

Disease Ontology Definition:A myopathy is characterized by progressive skeletal muscle weakness degeneration.

Synonyms:

Xenbase Genes : popdc1, syne2, flnc, hnrnpdl, dmd.2, cnbp, lmna, gmppb, sgcb, pomt1, sgcd, dmpk, lama2, tor1aip1, emd, [+]

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0020121 - muscular dystrophy

MIM:
MIM:158800 - MUSCULAR DYSTROPHY, BARNES TYPE
MIM:159050 - MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC, WITH INTERNALIZED CAPILLARIES
MIM:309930 - MUSCULAR DYSTROPHY, CARDIAC TYPE
MIM:309950 - MUSCULAR DYSTROPHY, HEMIZYGOUS LETHAL TYPE
MIM:310000 - MUSCULAR DYSTROPHY, MABRY TYPE
MIM:310095 - MUSCULAR DYSTROPHY, PROGRESSIVE PECTORODORSAL
MIM:600416 - MUSCULAR DYSTROPHY, SCAPULOHUMERAL

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Brody myopathy (is_a), myopathy (is_a)