Hemoglobin H disease
| Hemoglobin H disease | |
|---|---|
| Other names | α-thalassemia intermedia |
| Specialty | Hematology |
Hemoglobin H disease, also called α-thalassemia intermedia, is a disease affecting hemoglobin, the oxygen carrying molecule within red blood cells. It is a form of α-thalassemia which most commonly occurs due to deletion of 3 out of 4 of the α-globin genes.