Limb-girdle muscular dystrophy 1E, gene mapped to 7q (Q84651): Difference between revisions
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Latest revision as of 09:59, 15 August 2026
Autosomal dominant limb-girdle muscular dystrophy type 1D belongs to a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved. LGMD 1D is transmitted as an autosomal dominant form.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_586397197 |
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| English | Limb-girdle muscular dystrophy 1E, gene mapped to 7q |
Autosomal dominant limb-girdle muscular dystrophy type 1D belongs to a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved. LGMD 1D is transmitted as an autosomal dominant form. |
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CID11:ID_586397197
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dki-india-ID_586397197
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Concluído
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13 August 2026
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