Term Name:	congenital muscular dystrophy due to LMNA mutation
Synonyms:	congenital muscular dystrophy LMNA-related, L-CMD, LMNA-related congenital muscular dystrophy
Definition:	A congenital muscular dystrophy characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the LMNA gene on chromosome 1q22.
Ontology:	Human Disease [DOID:0110640]   ( DOID:0110640 )