3B61.0Y

ICD-11 MMS 2026-01

Other specified hereditary thrombophilia

Inclusions

  • Hereditary thrombophilia due to activated protein C resistance
  • Hereditary thrombophilia due to congenital antithrombin deficiency
  • Hereditary thrombophilia due to congenital protein S deficiency
  • Hereditary thrombophilia due to congenital protein C deficiency
  • Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency

Exclusions from above levels

  • JA43.3 – Postpartum coagulation defects
  • 04 – Diseases of the immune system
  • 05 – Endocrine, nutritional or metabolic diseases
Show allHide
  • 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

  • 3B61.00 – Hyperhomocysteinaemia
  • 3B61.0Z – Hereditary thrombophilia, unspecified

Foundation entity

Hereditary thrombophilia – http://id.who.int/icd/entity/535489185

Part of: 3B61.0: Hereditary thrombophilia › 3B61: Thrombophilia › 03: Diseases of the blood or blood-forming organs