Haemoglobin H disease (– α/– – included) (Q39514): Difference between revisions
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| description / pt-br | description / pt-br | ||
Doença da hemoglobina H (HbH) é uma forma moderada a grave da alfa talassemia caracterizada por anemia hemolítica hipocrômica microcítica acentuada. | |||
| description / en | description / en | ||
Haemoglobin H (HbH) disease is a moderate to severe form of alpha-thalassemia characterised by pronounced microcytic hypochromic haemolytic anaemia. | |||
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. |
