Hereditary factor VIII deficiency (Q39575): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Doença causada por uma mutação geneticamente herdada levando a uma deficiência na coagulação devida à falta de fator VIII. Essa doença é caracterizada por aumento na ocorrência de hemorragias e equimoses. A confirmação é feita por identificação de mutações por testagem genética.
@@ description / en / description / en @@
+A disease caused by a genetically inherited mutation leading to a deficiency in clotting due to lack of factor VIII. This disease is characterised by increasing haemorrhaging and bruising. Confirmation is by identification of mutations by genetic testing.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1573164739
@@ Property / Canonical URI: https://id.who.int/icd/entity/1573164739 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:3B10
@@ Property / CURIE: CID11:3B10 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-3B10
@@ Property / Canary Token: dki-india-3B10 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank
@@ Property / Linked ICD 10 @@
+D66
@@ Property / Linked ICD 10: D66 / rank @@
+Normal rank

Latest revision as of 05:03, 13 August 2026

A disease caused by a genetically inherited mutation leading to a deficiency in clotting due to lack of factor VIII. This disease is characterised by increasing haemorrhaging and bruising. Confirmation is by identification of mutations by genetic testing.

Language	Label	Description	Also known as
default for all languages	3B10
English	Hereditary factor VIII deficiency	A disease caused by a genetically inherited mutation leading to a deficiency in clotting due to lack of factor VIII. This disease is characterised by increasing haemorrhaging and bruising. Confirmation is by identification of mutations by genetic testing.