Any muscular dystrophy in which the cause of the disease is a mutation in the LAMA2 gene. [ https://clinicalgenome.org/affiliation/40031/ http://www.ncbi.nlm.nih.gov/pubmed/30055037 ]
Synonyms: LAMA2-related muscular dystrophy
Term information
- UMLS:C5679788 (MONDO:equivalentTo)
- MEDGEN:1826054 (MONDO:equivalentTo)
gard_rare, otar, rare, clingen
http://identifiers.org/medgen/1826054
http://linkedlifedata.com/resource/umls/id/C5679788