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

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C5679788 (MONDO:equivalentTo)
  • MEDGEN:1826054 (MONDO:equivalentTo)
Subsets

gard_rare, otar, rare, clingen

ClinGen label
LAMA2-related muscular dystrophy

creator

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

exactMatch

http://identifiers.org/medgen/1826054

http://linkedlifedata.com/resource/umls/id/C5679788

id

MONDO:0100228