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Metadata
ID	DOID:0110303
Name	autosomal dominant limb-girdle muscular dystrophy type 1H
Definition	An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in variation in the region 3p25.1-p23. https://www.ncbi.nlm.nih.gov/pubmed/20068593
Xrefs	ICD10CM:G71.0 MIM:613530 ORDO:238755
Subsets	DO_rare_slim
Synonyms	muscular dystrophy limb-girdle type 1H [EXACT]
Parent Relationships	is_a autosomal dominant limb-girdle muscular dystrophy