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autosomal dominant limb-girdle muscular dystrophy type 1H (DOID:0110303)
Alliance: disease page
Synonyms: LGMD1H; muscular dystrophy limb-girdle type 1H
Alt IDs: OMIM:613530, ICD10CM:G71.0, ORDO:238755
Definition: An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in with variation in the region 3p25.1-p23.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.11
The Jackson Laboratory