Any muscular dystrophy in which the cause of the disease is a mutation in the LAMA2 gene. [ http://www.ncbi.nlm.nih.gov/pubmed/30055037 https://clinicalgenome.org/affiliation/40031/ ]

Synonyms: LAMA2-related muscular dystrophy

This is just here as a test because I lose it

Term information

Subsets

otar, rare, inferred_rare

ClinGen label
LAMA2-related muscular dystrophy

creator

https://orcid.org/0000-0001-5208-3432

id

MONDO:0100228