6p24pter deletion (Q101706): 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 monossomia distal 6p é responsável por uma síndrome de deleção cromossômica distinta com um quadro clínico reconhecível, incluindo déficit intelectual, anormalidades oculares que afetam principalmente a câmara anterior do olho, perda auditiva e dismorfismo facial.
description / endescription / en
 
Distal monosomy 6p is responsible for a distinct chromosome deletion syndrome with a recognizable clinical picture including intellectual deficit, ocular abnormalities that mainly affect the anterior chamber of the eye, hearing loss, and facial dysmorphism.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1452973874 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_1452973874
Property / CURIE: CID11:ID_1452973874 / rank
 
Normal rank
Property / Canary Token
 
dki-india-ID_1452973874
Property / Canary Token: dki-india-ID_1452973874 / 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
 
15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 15 August 2026 / rank
 
Normal rank

Latest revision as of 18:33, 16 August 2026

Distal monosomy 6p is responsible for a distinct chromosome deletion syndrome with a recognizable clinical picture including intellectual deficit, ocular abnormalities that mainly affect the anterior chamber of the eye, hearing loss, and facial dysmorphism.
Language Label Description Also known as
default for all languages
ID_1452973874
    English
    6p24pter deletion
    Distal monosomy 6p is responsible for a distinct chromosome deletion syndrome with a recognizable clinical picture including intellectual deficit, ocular abnormalities that mainly affect the anterior chamber of the eye, hearing loss, and facial dysmorphism.

      Statements

      CID11:ID_1452973874
      0 references
      dki-india-ID_1452973874
      0 references
      Concluído
      0 references
      15 August 2026
      0 references