Congenital thrombocytopenia

Description

A disease caused by determinants arising during the antenatal period leading to low platelet count. This disease is characterised by decreased levels of platelets within the blood. This disease may present with increased bruising or haemorrhaging. Confirmation is by identification of a decreased platelet count 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

3B64.00 – Congenital non-inherited thrombocytopenia
3B64.01 – Hereditary thrombocytopenia
3B64.0Z – Congenital thrombocytopenia, unspecified

Sibling codes

3B64.1 – Acquired thrombocytopenia
3B64.Z – Thrombocytopenia, unspecified

Foundation entity

Congenital thrombocytopenia – http://id.who.int/icd/entity/672733376

Part of: 3B64: Thrombocytopenia › 03: Diseases of the blood or blood-forming organs