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Summary Literature (12)
DOID:9884 - muscular dystrophy


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

Synonyms:

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

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : syne2, flnc, dmd.2, cnbp, lmna, gmppb, sgcb, pomt1, sgcd, dmpk, lama2, emd, myot, sgcg, pomgnt1, [+]

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): myopathy (is_a)


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