Inherited coagulation factor deficiency without bleeding tendency (Q39583): Difference between revisions

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description / pt-brdescription / pt-br
 
Doença causada por uma mutação geneticamente herdada levando a níveis diminuídos de fator da coagulação. Essa doença é caracterizada por níveis diminuídos de fator da coagulação sem levar a aumento de hemorragias. A confirmação é feita pela identificação de níveis diminuídos de fator da coagulação em amostra de sangue.
description / endescription / en
 
A disease caused by a genetically inherited mutation leading to decreased levels of coagulation factor. This disease is characterised by decreased levels of coagulation factor without leading to increased haemorrhaging. Confirmation is by identification of decreased levels of coagulation factor in a blood sample.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1795705470 / rank
 
Normal rank
Property / CURIE
 
CID11:3B15
Property / CURIE: CID11:3B15 / rank
 
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Property / Canary Token
 
dki-india-3B15
Property / Canary Token: dki-india-3B15 / 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
 
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Latest revision as of 05:03, 13 August 2026

A disease caused by a genetically inherited mutation leading to decreased levels of coagulation factor. This disease is characterised by decreased levels of coagulation factor without leading to increased haemorrhaging. Confirmation is by identification of decreased levels of coagulation factor in a blood sample.
Language Label Description Also known as
default for all languages
3B15
    English
    Inherited coagulation factor deficiency without bleeding tendency
    A disease caused by a genetically inherited mutation leading to decreased levels of coagulation factor. This disease is characterised by decreased levels of coagulation factor without leading to increased haemorrhaging. Confirmation is by identification of decreased levels of coagulation factor in a blood sample.

      Statements

      CID11:3B15
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      dki-india-3B15
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      Concluído
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      13 August 2026
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