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Summary Literature (0)
DOID:0110301 - autosomal dominant limb-girdle muscular dystrophy type 1B


Disease Ontology Definition:An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in mutation in the gene encoding lamin A/C (LMNA).

Synonyms: LGMD1B, Limb-girdle muscular dystrophy due to lamin A/C deficiency, muscular dystrophy, limb-girdle type 1B, proximal muscular dystrophy type 1B

Referenced OMIM:
OMIM:159001 - MOVED TO 181350

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

Xenbase Genes : lmna

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant limb-girdle muscular dystrophy (is_a)


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