Haemoglobin H disease (– α/– – included) (Q39514): 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/9436211 / rank | |||
Normal rank | |||
Revision as of 04:57, 13 August 2026
Haemoglobin H (HbH) disease is a moderate to severe form of alpha-thalassemia characterised by pronounced microcytic hypochromic haemolytic anaemia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A50.02 |
||
| English | Haemoglobin H disease (– α/– – included) |
Haemoglobin H (HbH) disease is a moderate to severe form of alpha-thalassemia characterised by pronounced microcytic hypochromic haemolytic anaemia. |
