Limb-girdle muscular dystrophy 2B, dysferlin deficiency (Q86047): 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-brdescription / pt-br
 
A distrofia muscular de cinturas autossômica recessiva (LGMD) tipo 2B é um tipo de LGMD, um grupo de distúrbios de fraqueza muscular progressiva, geneticamente determinados, em que a musculatura pélvica ou da cintura escapular está predominantemente ou principalmente envolvida e é caracterizada por pequena cintura escapular envolvimento e envolvimento da panturrilha.
description / endescription / en
 
Autosomal recessive limb-girdle muscular dystrophy (LGMD) type 2B is a type of LGMD, a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved, and is characterised by little shoulder girdle involvement and calf involvement.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/370913678 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_370913678
Property / CURIE: CID11:ID_370913678 / rank
 
Normal rank
Property / Canary Token
 
dki-india-ID_370913678
Property / Canary Token: dki-india-ID_370913678 / 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
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
Normal rank

Latest revision as of 11:24, 15 August 2026

Autosomal recessive limb-girdle muscular dystrophy (LGMD) type 2B is a type of LGMD, a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved, and is characterised by little shoulder girdle involvement and calf involvement.
Language Label Description Also known as
default for all languages
ID_370913678
    English
    Limb-girdle muscular dystrophy 2B, dysferlin deficiency
    Autosomal recessive limb-girdle muscular dystrophy (LGMD) type 2B is a type of LGMD, a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved, and is characterised by little shoulder girdle involvement and calf involvement.

      Statements

      CID11:ID_370913678
      0 references
      dki-india-ID_370913678
      0 references
      Concluído
      0 references
      13 August 2026
      0 references