autosomal dominant Emery-Dreifuss muscular dystrophy 2 (Q60195098)
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Emery-Dreifuss muscular dystrophy that has material basis in an autosomal dominant mutation of LMNA on chromosome 1q22
- Emery-Dreifuss muscular dystrophy 2, autosomal dominant
- EMD2
- scapuloilioperoneal atrophy with cardiopathy
- Emery-Dreifuss muscular dystrophy, autosomal dominant
- EDMD2
- muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant
- Hauptmann-Thannhauser muscular dystrophy
- autosomal dominant limb-girdle muscular dystrophy type 1B
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant Emery-Dreifuss muscular dystrophy 2 |
Emery-Dreifuss muscular dystrophy that has material basis in an autosomal dominant mutation of LMNA on chromosome 1q22 |
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Identifiers
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1 reference