LAMA2-related muscular dystrophy
MONDO:0100228Mondo
Findings
No curated finding names LAMA2-related muscular dystrophy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any muscular dystrophy in which the cause of the disease is a mutation in the LAMA2 gene.
Definition from the Mondo Disease Ontology (MONDO:0100228), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- LAMA2HGNC:6482
- Definitive · ClinGen · Autosomal recessive · 2022
- Strong · PanelApp Australia · Autosomal recessive · 2025