facioscapulohumeral muscular dystrophy

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Summary

Literature (2)

DOID:11727 - facioscapulohumeral muscular dystrophy

Disease Ontology Definition:n_a

Synonyms: Landouzy Dejerine muscular dystrophy, Landouzy-Dejerine muscular dystrophy, Muscular dystrophy, Landouzy-Dejerine,

Xenbase 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

: smchd1, frg1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0001347 - facioscapulohumeral muscular dystrophy

MONDO:0001347 - facioscapulohumeral muscular dystrophy

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

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

Parent(s): muscular dystrophy (is_a)