Mild haemophilia B (Q89214): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed an Item
‎Changed an Item
 
(3 intermediate revisions by the same user not shown)
Property / Canary Token
 
dki-india-ID_1810106678
Property / Canary Token: dki-india-ID_1810106678 / 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
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
Normal rank

Latest revision as of 15:47, 15 August 2026

Mild haemophilia B is a form of haemophilia B characterised by a small deficiency of factor IX leading to abnormal bleeding as a result of minor injuries, or following surgery or tooth extraction. Mild haemophilia B accounts for around 30% of all cases of haemophilia B. The biological activity of factor IX is between 5 and 40%. Spontaneous haemorrhages do not occur. Transmission is X-linked recessive and the disorder is caused by mutations in the F9 gene (Xq28) encoding coagulation factor IX.
Language Label Description Also known as
default for all languages
ID_1810106678
    English
    Mild haemophilia B
    Mild haemophilia B is a form of haemophilia B characterised by a small deficiency of factor IX leading to abnormal bleeding as a result of minor injuries, or following surgery or tooth extraction. Mild haemophilia B accounts for around 30% of all cases of haemophilia B. The biological activity of factor IX is between 5 and 40%. Spontaneous haemorrhages do not occur. Transmission is X-linked recessive and the disorder is caused by mutations in the F9 gene (Xq28) encoding coagulation factor IX.

      Statements

      CID11:ID_1810106678
      0 references
      dki-india-ID_1810106678
      0 references
      Concluído
      0 references
      13 August 2026
      0 references