congenital muscular dystrophy due to LMNA mutation (DOID:0110640)
Alliance: disease page
Synonyms: congenital muscular dystrophy LMNA-related; L-CMD; LMNA-related congenital muscular dystrophy
Alt IDs: OMIM:613205, ICD10CM:G71.2, ORDO:157973
Definition: A congenital muscular dystrophy characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the LMNA gene on chromosome 1q22.