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Metadata
ID	DOID:0111217
Name	autosomal dominant centronuclear myopathy
Definition	A centronuclear myopathy that has_material_basis_in autosomal dominant inheritance. https://www.ncbi.nlm.nih.gov/pubmed/30103348
Xrefs	GARD:12719 ICD10CM:G71.228 MESH:D020914 ORDO:169189 SNOMEDCT_US_2023_03_01:716696006 UMLS_CUI:C1834558
Subsets	DO_rare_slim
Synonyms	AD-CNM [EXACT]
Parent Relationships	is_a centronuclear myopathy is_a autosomal dominant disease