3B50.Z

ICD-11 MMS 2026-01

Inherited fibrinolytic defects, unspecified

Exclusions from above levels

  • JA43.3 – Postpartum coagulation defects
  • 04 – Diseases of the immune system
  • 05 – Endocrine, nutritional or metabolic diseases
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  • 18 – Complications of pregnancy, childbirth or the puerperium
  • 19 – Certain conditions originating in the perinatal period
  • 20 – Congenital malformations, deformations or chromosomal abnormalities
  • 22 – Injury, poisoning or certain other consequences of external causes
  • http://id.who.int/icd/entity/1000704511 – Human immunodeficiency virus disease
  • JB64.1 – Other diseases of the blood or blood-forming organs or certain disorders involving the immune mechanism complicating pregnancy, childbirth or the puerperium

Sibling codes

  • 3B50.0 – Congenital alpha-2 antiplasmin deficiency
  • 3B50.1 – Congenital plasminogen activator inhibitor type 1 deficiency
  • 3B50.Y – Other specified inherited fibrinolytic defects

Foundation entity

Inherited fibrinolytic defects – http://id.who.int/icd/entity/1502898025

Part of: 3B50: Inherited fibrinolytic defects › 03: Diseases of the blood or blood-forming organs