bn:04916035n
Noun Named Entity
Categories: Blood disorders
EN
Hemoglobin H disease  alpha-thalassemia intermedia  alpha thalassemia, hemoglobin H type  HBH  hemoglobin H
EN
Hemoglobin H Disease, also called alpha-thalassemia intermedia, is a disease affecting hemoglobin, the oxygen carrying molecule within red blood cells. Wikipedia
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EN
Hemoglobin H Disease, also called alpha-thalassemia intermedia, is a disease affecting hemoglobin, the oxygen carrying molecule within red blood cells. Wikipedia
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 Wikidata