Preferred Name | hemoglobin H disease | |
Synonyms |
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Definitions |
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. |
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ID |
http://purl.obolibrary.org/obo/DOID_0110031 |
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definition |
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. |
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imported from | ||
label |
hemoglobin H disease |
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prefixIRI |
DOID:0110031 |
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prefLabel |
hemoglobin H disease |
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subClassOf |
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