Hereditary thrombophilia

Description

A disease caused by hereditary factors leading to abnormalities in blood. This disease is characterised by abnormality of blood coagulation that increases the risk of thrombosis, clots in blood vessels. This disease may present with deep vein thrombosis or pulmonary embolism. Confirmation is identification of abnormal blood coagulation in a blood sample.

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

Child codes

3B61.00 – Hyperhomocysteinaemia
3B61.0Y – Other specified hereditary thrombophilia
3B61.0Z – Hereditary thrombophilia, unspecified

Sibling codes

3B61.1 – Acquired thrombophilia
3B61.Y – Other specified thrombophilia
3B61.Z – Thrombophilia, unspecified

Foundation entity

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

Part of: 3B61: Thrombophilia › 03: Diseases of the blood or blood-forming organs