autosomal recessive limb-girdle muscular dystrophy type 2W

Summary

DOID:0110288 - autosomal recessive limb-girdle muscular dystrophy type 2W

Disease Ontology Definition:An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in compound heterozygous mutation in the LIM zinc finger domain containing 2 gene (LIMS2) on chromosome 2q14.

Synonyms: LGMD2W, muscular dystrophy, limb-girdle, type 2W,

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

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Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014788 - autosomal recessive limb-girdle muscular dystrophy type 2W

MONDO:0014788 - autosomal recessive limb-girdle muscular dystrophy type 2W

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

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

Parent(s): autosomal recessive limb-girdle muscular dystrophy (is_a)