Limb-girdle muscular dystrophy 1H, gene mapped to 3p25.1p23 (Q84662): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed an Item |
||||||||||||||
| (6 intermediate revisions by the same user not shown) | |||||||||||||||
| description / pt-br | description / pt-br | ||||||||||||||
A distrofia muscular de cinturas tipo 1H (LGMD1H) é uma doença autossômica dominante caracterizada pelo início adulto de fraqueza muscular proximal progressiva que afeta os membros superiores e inferiores. Um locus de doença candidato, dentro de uma região de 25 cM no cromossomo 3p25.1-p23, foi identificado. | |||||||||||||||
| description / en | description / en | ||||||||||||||
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. | |||||||||||||||
| Property / Canonical URI | |||||||||||||||
| Property / Canonical URI: https://id.who.int/icd/entity/320673324 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:ID_320673324 | |||||||||||||||
| Property / CURIE: CID11:ID_320673324 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-ID_320673324 | |||||||||||||||
| Property / Canary Token: dki-india-ID_320673324 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
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 |
||
| 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. |
Statements
CID11:ID_320673324
0 references
dki-india-ID_320673324
0 references
Concluído
0 references
13 August 2026
0 references
