Other inherited coagulation factor deficiency with bleeding tendency (Q39584): Difference between revisions

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description / pt-brdescription / pt-br
 
Qualquer doença causada por mutações geneticamente herdadas levando à falta de fatores da coagulação no sangue não classificada em outra parte. Essas doenças são caracterizadas pela ocorrência aumentada de hemorragias e equimoses, pois o sangue não coagula adequadamente para controlar o sangramento. A confirmação é feita pela identificação de mutações por testagem genética.
description / endescription / en
 
Any disease caused by genetically inherited mutations leading to lack of coagulation factors in the blood not elsewhere classified. These diseases are characterised by increased haemorrhaging and bruising as the blood cannot clot properly to control bleeding. Confirmation is identification of mutations by genetic testing.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/573771682 / rank
 
Normal rank
Property / CURIE
 
CID11:3B14
Property / CURIE: CID11:3B14 / rank
 
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Property / Canary Token
 
dki-india-3B14
Property / Canary Token: dki-india-3B14 / rank
 
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Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
Normal rank
Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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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
 
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Property / Linked ICD 10
 
Property / Linked ICD 10: D68.2 / rank
 
Normal rank

Latest revision as of 05:04, 13 August 2026

Any disease caused by genetically inherited mutations leading to lack of coagulation factors in the blood not elsewhere classified. These diseases are characterised by increased haemorrhaging and bruising as the blood cannot clot properly to control bleeding. Confirmation is identification of mutations by genetic testing.
Language Label Description Also known as
default for all languages
3B14
    English
    Other inherited coagulation factor deficiency with bleeding tendency
    Any disease caused by genetically inherited mutations leading to lack of coagulation factors in the blood not elsewhere classified. These diseases are characterised by increased haemorrhaging and bruising as the blood cannot clot properly to control bleeding. Confirmation is identification of mutations by genetic testing.

      Statements

      CID11:3B14
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      dki-india-3B14
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      Concluído
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      13 August 2026
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      0 references