Fish-eye disease (Q106503): 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 doença do olho do peixe é uma forma de deficiência genética lecitina-colesterol aciltransferase (LCAT) caracterizada clinicamente por opacificações da córnea e bioquimicamente por colesterol HDL significativamente reduzido e deficiência parcial da enzima LCAT.
description / endescription / en
 
Fish eye disease (FED) is a form of genetic LCAT (lecithin-cholesterol acyltransferase) deficiency characterised clinically by corneal opacifications, and biochemically by significantly reduced HDL cholesterol and partial LCAT enzyme deficiency.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1737717544 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_1737717544
Property / CURIE: CID11:ID_1737717544 / rank
 
Normal rank
Property / Canary Token
 
dki-india-ID_1737717544
Property / Canary Token: dki-india-ID_1737717544 / 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
 
16 August 2026
Timestamp+2026-08-16T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 16 August 2026 / rank
 
Normal rank

Latest revision as of 13:29, 17 August 2026

Fish eye disease (FED) is a form of genetic LCAT (lecithin-cholesterol acyltransferase) deficiency characterised clinically by corneal opacifications, and biochemically by significantly reduced HDL cholesterol and partial LCAT enzyme deficiency.
Language Label Description Also known as
default for all languages
ID_1737717544
    English
    Fish-eye disease
    Fish eye disease (FED) is a form of genetic LCAT (lecithin-cholesterol acyltransferase) deficiency characterised clinically by corneal opacifications, and biochemically by significantly reduced HDL cholesterol and partial LCAT enzyme deficiency.

      Statements

      CID11:ID_1737717544
      0 references
      dki-india-ID_1737717544
      0 references
      Concluído
      0 references
      16 August 2026
      0 references