autosomal dominant limb-girdle muscular dystrophy

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Summary

Literature (0)

DOID:0110273 - autosomal dominant limb-girdle muscular dystrophy

Disease Ontology Definition:A limb-girdle muscular dystrophy that has_material_basis_in autosomal dominant inheritance.

Synonyms:

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

: hnrnpdl, lmna, dnajb6, tnpo3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0015151 - muscular dystrophy, limb-girdle, autosomal dominant

MONDO:0015151 - muscular dystrophy, limb-girdle, autosomal dominant

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), limb-girdle muscular dystrophy (is_a)