Qualitative platelet defects

Description

A disease caused by determinants arising after birth, during the antenatal period or genetically inherited factors. This disease is characterised by abnormalities in coagulation of the blood due to defective platelets. This condition may present with easy bruising, prolonged bleeding or bleeding gums. Confirmation is by identification of decreased platelets in a blood sample.

Inclusions

Thrombocytopathy

Excludes

3B12 – Von Willebrand disease

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

3B62.0 – Inherited qualitative platelet defects
3B62.1 – Bleeding diathesis due to thromboxane synthesis deficiency
3B62.2 – Isolated thrombocytopenia
3B62.3 – Dense granule disease
3B62.4 – Alpha-delta dense granule deficiency
3B62.Y – Other specified qualitative platelet defects
3B62.Z – Qualitative platelet defects, unspecified

Sibling codes

3B60 – Non-thrombocytopenic purpura
3B61 – Thrombophilia
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

Qualitative platelet defects – http://id.who.int/icd/entity/72474955

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