Inherited qualitative platelet defects

Description

A disease caused by genetically inherited mutations leading to abnormalities in platelets. This disease is characterised by abnormal platelet formation or function. Confirmation is by identification of mutations by genetic testing.

Exclusions from above levels

3B12 – Von Willebrand disease
JA43.3 – Postpartum coagulation defects
04 – Diseases of the immune system

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05 – Endocrine, nutritional or metabolic diseases
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

3B62.00 – Alpha-granule diseases
3B62.01 – Inherited giant platelet disorder
3B62.0Y – Other specified inherited qualitative platelet defects
3B62.0Z – Inherited qualitative platelet defects, unspecified

Foundation children elsewhere

3B62.3 – Dense granule disease
3B62.4 – Alpha-delta dense granule deficiency

Sibling codes

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

Foundation entity

Inherited qualitative platelet defects – http://id.who.int/icd/entity/1410128892

Part of: 3B62: Qualitative platelet defects › 03: Diseases of the blood or blood-forming organs