| 词条 | Hemoglobin H disease |
| 释义 |
| name = {{PAGENAME}} | synonyms = Alpha-thalassemia intermedia | image = | alt = | caption = | pronounce = | field = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }}Hemoglobin H disease is a type of alpha thalassemia caused by impaired production of three of the four alpha globins, coded by genes HBA1 and HBA2.[1] References1. ^{{Cite web|url=http://www.uptodate.com/contents/pathophysiology-of-alpha-thalassemia|title=Pathophysiology of alpha thalassemia|website=www.uptodate.com|access-date=2016-08-30}} External links{{Medical resources| ICD10 = D56.0 | ICD9 = | ICDO = | OMIM = 613978 | DiseasesDB = | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeSH = | GeneReviewsNBK = | GeneReviewsName = | Orphanet = 93616 }}{{Disease-stub}} 1 : Blood disorders |
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