Human genes for hemoglobin H disease
Hemoglobin H disease [DOID:0110031]
An alpha thalassemia that has_material_basis_in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other.
Synonyms: hemoglobin H disease, DOID:0110031, hemoglobin H disorder, hemoglobin H syndrome, hemoglobin H diseases ...