Thrombophilia

Description

A disease caused by determinants arising after birth or genetically inherited 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

3B61.0 – Hereditary thrombophilia
3B61.1 – Acquired thrombophilia
3B61.Y – Other specified thrombophilia
3B61.Z – Thrombophilia, unspecified

Sibling codes

3B60 – Non-thrombocytopenic purpura
3B62 – Qualitative platelet defects
3B63 – Thrombocytosis
3B64 – Thrombocytopenia
3B65 – Thrombotic microangiopathy, not elsewhere classified
3B6Y – Other specified coagulation defects, purpura or other haemorrhagic or related conditions
3B6Z – Coagulation defects, purpura or other haemorrhagic or related conditions, unspecified

Foundation entity

Thrombophilia – http://id.who.int/icd/entity/1733531851

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