lamin A/C congenital muscular dystrophy (Q27835675)
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congenital muscular dystrophy characterized by autosomal dominant inheritance that has material basis in heterozygous mutation in the LMNA gene on chromosome 1q22
- congenital muscular dystrophy due to LMNA mutation
- LMNA-related congenital muscular dystrophy
- congenital muscular dystrophy LMNA-related
- L-CMD
- MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED
- Mdcl
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | lamin A/C congenital muscular dystrophy |
congenital muscular dystrophy characterized by autosomal dominant inheritance that has material basis in heterozygous mutation in the LMNA gene on chromosome 1q22 |
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