Congenital pure red cell aplasia

Description

A condition caused by determinants arising during the antenatal period, leading to a change in the formation of erythrocytes. This condition is characterised by maturation arrest occurring in the formation of erythrocytes. This condition may present with severe anaemia. Confirmation is by identification of decreased red blood cell count in a blood sample.

Exclusions from above levels

04 – Diseases of the immune system
05 – Endocrine, nutritional or metabolic diseases
18 – Complications of pregnancy, childbirth or the puerperium

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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

3A60.0 – Congenital non-inherited pure red cell aplasia
3A60.1 – Hereditary pure red cell aplasia
3A60.Z – Congenital pure red cell aplasia, unspecified

Sibling codes

3A61 – Acquired pure red cell aplasia
3A6Z – Pure red cell aplasia, unspecified

Foundation entity

Congenital pure red cell aplasia – http://id.who.int/icd/entity/217030515

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