Hereditary pure red cell aplasia (Q39554): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (One intermediate revision by the same user not shown) | |||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Linked ICD 10 | |||||||||||||||
| Property / Linked ICD 10: D61.0 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 05:01, 13 August 2026
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 occuring 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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A60.1 |
||
| English | Hereditary pure red cell aplasia |
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 occuring 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. |
Statements
CID11:3A60.1
0 references
dki-india-3A60.1
0 references
Concluído
0 references
13 August 2026
0 references
