Limb-girdle muscular dystrophy 2H, TRIM32 gene mutation (Q86057): 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 (LGMD) 2H pertence a um grupo de distúrbios de fraqueza muscular progressiva, geneticamente determinados, nos quais a musculatura pélvica ou da cintura escapular está predominantemente ou principalmente envolvida. LGMD 2H é transmitido como uma forma autossômica recessiva. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Limb girdle muscular dystrophy (LGMD) 2H 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 2H is transmitted as an autosomal recessive form. | |||||||||||||||
| Property / Canonical URI | |||||||||||||||
| Property / Canonical URI: https://id.who.int/icd/entity/2020366790 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:ID_2020366790 | |||||||||||||||
| Property / CURIE: CID11:ID_2020366790 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-ID_2020366790 | |||||||||||||||
| Property / Canary Token: dki-india-ID_2020366790 / 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 11:25, 15 August 2026
Limb girdle muscular dystrophy (LGMD) 2H 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 2H is transmitted as an autosomal recessive form.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2020366790 |
||
| English | Limb-girdle muscular dystrophy 2H, TRIM32 gene mutation |
Limb girdle muscular dystrophy (LGMD) 2H 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 2H is transmitted as an autosomal recessive form. |
Statements
CID11:ID_2020366790
0 references
dki-india-ID_2020366790
0 references
Concluído
0 references
13 August 2026
0 references
