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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,
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee