" /> Hereditary pure red cell aplasia - CISMeF





ICD-11 code : 3A60.1;

Preferred Label : Hereditary pure red cell aplasia;

ICD-11 definition : A condition caused by determinates arising during the antenatal period, leading to a change in the formation of erythrocytes. This condition is characterised by maturation arrest occurs 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.;

ICD-11 synonym : Familial hypoplastic anaemia with malformations; Constitutional pure red cell aplasia;

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A condition caused by determinates arising during the antenatal period, leading to a change in the formation of erythrocytes. This condition is characterised by maturation arrest occurs 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.

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01/05/2025


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