Inherited fibrinolytic defects (Q39608): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Doença causada por mutações geneticamente herdadas que afetam o sistema de fibrinólise que evita que coágulos sanguíneos se estendam e se tornem problemáticos. Essa doença é caracterizada por defeitos no sistema de fibrinólise, levando à coagulação do sangue. Pode apresentar-se com trombose.
@@ description / en / description / en @@
+A disease caused by genetically inherited mutations affecting the fibrinolysis system which prevents blood clots from growing and becoming problematic. This disease is characterised by defects in the fibrinolysis system leading to coagulation of the blood. This disease may present with thrombosis.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1502898025
@@ Property / Canonical URI: https://id.who.int/icd/entity/1502898025 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:3B50
@@ Property / CURIE: CID11:3B50 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-3B50
@@ Property / Canary Token: dki-india-3B50 / 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 @@
+D68.8
@@ Property / Linked ICD 10: D68.8 / rank @@
+Normal rank

Latest revision as of 05:05, 13 August 2026

A disease caused by genetically inherited mutations affecting the fibrinolysis system which prevents blood clots from growing and becoming problematic. This disease is characterised by defects in the fibrinolysis system leading to coagulation of the blood. This disease may present with thrombosis.

Language	Label	Description	Also known as
default for all languages	3B50
English	Inherited fibrinolytic defects	A disease caused by genetically inherited mutations affecting the fibrinolysis system which prevents blood clots from growing and becoming problematic. This disease is characterised by defects in the fibrinolysis system leading to coagulation of the blood. This disease may present with thrombosis.