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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.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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11/12/2024
MGI 6.24 		The Jackson Laboratory