Hereditary haemolytic anaemia due to enzyme deficiency (Q59910): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/1728186890 / rank | |||
Normal rank | |||
Revision as of 07:25, 14 August 2026
A disease caused by low levels of certain enzymes in the body leading to premature destruction of red blood cells in the antenatal period. This disease is characterised by low levels of red blood cells in the body due to abnormal destruction of the cells. A decrease in red blood cell mass due to premature destruction of erythrocytes in the spleen or peripheral vessels secondary to G6PD or other enzyme deficiency. This disease may present with pallor, fatigue, or shortness of breath.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1728186890 |
||
| English | Hereditary haemolytic anaemia due to enzyme deficiency |
A disease caused by low levels of certain enzymes in the body leading to premature destruction of red blood cells in the antenatal period. This disease is characterised by low levels of red blood cells in the body due to abnormal destruction of the cells. A decrease in red blood cell mass due to premature destruction of erythrocytes in the spleen or peripheral vessels secondary to G6PD or other enzyme deficiency. This disease may present with pallor, fatigue, or shortness of breath. |
