Dilated cardiomyopathy due to iron overload (Q98625): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed label, description and/or aliases in pt-br, en
‎Changed an Item
 
(5 intermediate revisions by the same user not shown)
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/808521772 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_808521772
Property / CURIE: CID11:ID_808521772 / rank
 
Normal rank
Property / Canary Token
 
dki-india-ID_808521772
Property / Canary Token: dki-india-ID_808521772 / 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 15:11, 16 August 2026

Dilated cardiomyopathy due to iron overload occurs either primarily due to a genetic predisposition to absorb and store iron in excess amounts (hereditary haemochromatosis), or secondarily as a complication of other haematologic disorders that require chronic transfusion therapy (such as sickle cell disease and thalassaemia), repeated injections of parenteral iron (such as for chronic kidney disease), or due to excessive iron ingestion. Additional information: Iron-overload cardiomyopathy in children and young adults with the above conditions begins as a restrictive cardiomyopathy with severe diastolic dysfunction, eventually progressing to end-stage dilated cardiomyopathy with mixed systolic and diastolic dysfunction.
Language Label Description Also known as
default for all languages
ID_808521772
    English
    Dilated cardiomyopathy due to iron overload
    Dilated cardiomyopathy due to iron overload occurs either primarily due to a genetic predisposition to absorb and store iron in excess amounts (hereditary haemochromatosis), or secondarily as a complication of other haematologic disorders that require chronic transfusion therapy (such as sickle cell disease and thalassaemia), repeated injections of parenteral iron (such as for chronic kidney disease), or due to excessive iron ingestion. Additional information: Iron-overload cardiomyopathy in children and young adults with the above conditions begins as a restrictive cardiomyopathy with severe diastolic dysfunction, eventually progressing to end-stage dilated cardiomyopathy with mixed systolic and diastolic dysfunction.

      Statements

      CID11:ID_808521772
      0 references
      dki-india-ID_808521772
      0 references
      Concluído
      0 references
      15 August 2026
      0 references