Hemoglobin D disease
ORPHA:90039· ICD-10 D58.2
Definition
Hemoglobin D disease(HbD) is a hemoglobinopathy characterized by production of abnormal variant hemoglobin known as hemoglobin D, with no or mild clinical manifestations (splenomegaly, very mild anemia).
- Prevalence
- Unknown
- Inheritance
- Autosomal recessive
- Age of onset
- Childhood