C185522Level 8
Hemoglobin Alpha Homozygous Null Genotype
**Semantic type:** Laboratory or Test Result
**Definition:** A genetic finding indicating that neither copy of chromosome 16 has any functional copies of the hemoglobin alpha (HBA) genes. This genotype is associated with hemoglobin Barts.
**Synonyms:** - (--/--) - --/-- - HBA Homozygous Null Genotype - HBA Null Genotype - Hemoglobin Alpha Null Genotype - alpha-globin genotype (- - / - - )
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