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  2. Alpha-thalassemia

Alpha-thalassemia

Disease Export to PDF
Name:
Alpha-thalassemia
Description:

An inherited hemoglobinopathy characterized by impaired synthesis of alpha-globin chains leading to a variable clinical picture depending on the number of affected alleles.
ORPHAcode:
846
XREF(s):
Orphanet
Created:
26 Jul 2019 - 09:58
Changed:
26 Jul 2019 - 09:58