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Hemoglobin H disease
rareAlpha thalassemia caused by variation in three of the four copies of the alpha hemoglobin genes (e.g., large deletion in HBA1 and HBA2 genes in trans with a variant in either HBA1 or HBA2).
- Identifiers
- MONDO:0013512 OMIM:613978Orphanet:93616
- Also known as
- Alpha-thalassemia intermedia · Alpha-thalassemia, Haemoglobin H type · Haemoglobin H disease, Deletional · haemoglobin H disease, deletional and nondeletional · Haemoglobin H disease, Nondeletional
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