Pure red cell aplasia
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
A condition caused by determinates arising during the antenatal period, after birth or genetically inherited factors, leading to a change in the formation of erythrocytes. This condition is characterised by maturation arrest occuring in the formation of erythrocytes. This condition may present with severe anaemia. Confirmation is by identification of abnormally formed erythrocytes in a blood sample.
sections/codes in this section (3A60-3A6Z)
- Congenital pure red cell aplasia (3A60)
- Acquired pure red cell aplasia (3A61)
- Pure red cell aplasia, unspecified (3A6Z)
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