ICD-11 classes
03 Diseases of the blood or blood-forming organs
Coagulation defects, purpura or other haemorrhagic or...
Fibrinolytic defects
3B50 — Inherited fibrinolytic defects
ICD-11 3B50 — 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.
The diagnosis includes nothing.
The diagnosis excludes nothing.
Diagnosis with code 3B50 contains 5 clarifying diagnoses:
- 3B50.0 — Congenital alpha-2 antiplasmin deficiency
- 3B50.1 — Congenital plasminogen activator inhibitor type 1 deficiency
- DA0D.3 — Hypoplasminogenaemia
- 3B50.Y — Other specified inherited fibrinolytic defects
- 3B50.Z — Inherited fibrinolytic defects, unspecified
The diagnosis is included in 1 another class.
- Hypoplasminogenaemia (DA0D.3)