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autosomal dominant limb-girdle muscular dystrophy type 1B (DOID:0110301)
Alliance: disease page
Synonyms: LGMD1B; Limb-girdle muscular dystrophy due to lamin A/C deficiency; muscular dystrophy, limb-girdle type 1B; proximal muscular dystrophy type 1B
Alt IDs: OMIM:159001, ICD10CM:G71.0, ORDO:264
Definition: An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in mutation in the gene encoding lamin A/C (LMNA).

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory