Limb-girdle muscular dystrophy 1H, gene mapped to 3p25.1p23 (Q84662): Difference between revisions
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13 August 2026
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Latest revision as of 10:00, 15 August 2026
Limb-girdle muscular dystrophy type 1H (LGMD1H) is an autosomal dominant disorder characterised by adult onset of progressive proximal muscle weakness affecting both the upper and lower limbs. A candidate disease locus, within a 25-cM region on chromosome 3p25.1-p23, has been identified.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_320673324 |
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| English | Limb-girdle muscular dystrophy 1H, gene mapped to 3p25.1p23 |
Limb-girdle muscular dystrophy type 1H (LGMD1H) is an autosomal dominant disorder characterised by adult onset of progressive proximal muscle weakness affecting both the upper and lower limbs. A candidate disease locus, within a 25-cM region on chromosome 3p25.1-p23, has been identified. |
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CID11:ID_320673324
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dki-india-ID_320673324
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Concluído
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13 August 2026
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