Other inherited coagulation factor deficiency with bleeding tendency (Q39584): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed an Item |
||||||||||||||
| (7 intermediate revisions by the same user not shown) | |||||||||||||||
| description / pt-br | description / 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 / en | description / 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 | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-3B14 | |||||||||||||||
| Property / Canary Token: dki-india-3B14 / 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
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| 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
0 references
dki-india-3B14
0 references
Concluído
0 references
13 August 2026
0 references
