Hemoglobin H disease

From Wikipedia, the free encyclopedia
  (Redirected from Hemoglobin H)
Jump to navigation Jump to search
Hemoglobin H disease
Other namesAlpha-thalassemia intermedia

Hemoglobin H disease is a type of alpha thalassemia caused by impaired production of three of the four alpha globins, coded by genes HBA1 and HBA2.[1]


  1. ^ "Pathophysiology of alpha thalassemia". www.uptodate.com. Retrieved 2016-08-30.

External links[edit]

External resources