Hereditary vitamin K-dependent coagulation factors deficiency (Q67792): Difference between revisions

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Doença causada por mutações geneticamente herdadas. Essa doença é caracterizada por níveis baixos de vitamina K no organismo, levando a anormalidades na coagulação sanguínea. Pode apresentar-se com sangramento prolongado e hemorragias. A confirmação é feita pela identificação de mutações por testagem genética.
description / endescription / en
 
A disease caused by genetically inherited mutations. This disease is characterised by low levels of vitamin K in the body leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding and haemorrhaging. Confirmation is by identification of mutations through genetic testing.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1818851075 / rank
 
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Property / CURIE
 
CID11:ID_1818851075
Property / CURIE: CID11:ID_1818851075 / rank
 
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Property / Canary Token
 
dki-india-ID_1818851075
Property / Canary Token: dki-india-ID_1818851075 / rank
 
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Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
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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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Latest revision as of 15:37, 14 August 2026

A disease caused by genetically inherited mutations. This disease is characterised by low levels of vitamin K in the body leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding and haemorrhaging. Confirmation is by identification of mutations through genetic testing.
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ID_1818851075
    English
    Hereditary vitamin K-dependent coagulation factors deficiency
    A disease caused by genetically inherited mutations. This disease is characterised by low levels of vitamin K in the body leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding and haemorrhaging. Confirmation is by identification of mutations through genetic testing.

      Statements

      CID11:ID_1818851075
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      dki-india-ID_1818851075
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      Concluído
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      13 August 2026
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