3B13

ICD-11 MMS 2026-01

Haemophilia C

Description

A disease caused by genetically inherited mutations. This disease is characterised by decreased levels of factor XI leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding, easy bruising or bleeding gums. Confirmation is by identification of mutation through genetic testing.

Index terms

  • Haemophilia C
  • PTA - [plasma thromboplastin antecedent] deficiency
  • Rosenthal disease
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  • Rosenthal factor deficiency
  • Rosenthal syndrome
  • congenital factor XI deficiency
  • congenital factor XI deficiency disease
  • factor XI deficiency
  • hereditary factor XI deficiency disease
  • plasma thromboplastin antecedent deficiency
  • thromboplastin antecedent deficiency

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

  • 3B10 – Hereditary factor VIII deficiency
  • 3B11 – Hereditary factor IX deficiency
  • 3B12 – Von Willebrand disease
  • 3B14 – Other inherited coagulation factor deficiency with bleeding tendency
  • 3B15 – Inherited coagulation factor deficiency without bleeding tendency
  • 3B1Z – Congenital or constitutional haemorrhagic condition, unspecified

Foundation entity

Haemophilia C – http://id.who.int/icd/entity/413739466

Part of: 03: Diseases of the blood or blood-forming organs