- HPFH
- hereditary persistence of fetal hemoglobin
Medical dictionary. 2011.
Medical dictionary. 2011.
HPFH — • hereditary persistence of fetal hemoglobin … Dictionary of medical acronyms & abbreviations
HBG1 — Hemoglobin, gamma A, also known as HBG1, is a human gene. PBB Summary section title = summary text = The gamma globin genes (HBG1 and HBG2) are normally expressed in the fetal liver, spleen and bone marrow. Two gamma chains together with two… … Wikipedia
Hereditary persistence of fetal hemoglobin — (HPFH, BrE: Hereditary persistence of foetal haemoglobin ) is a benign condition in which significant fetal hemoglobin (hemoglobin F) production continues well into adulthood, disregarding the normal shutoff point after which only adult type… … Wikipedia
Haemophilia — Classification and external resources Deficiency in coagulation factor VIII is the most common cause of haemophilia. ICD 10 D … Wikipedia
Haematopoiesis — Diagram showing the development of different blood cells from haematopoietic stem cell to mature cells Haematopoiesis (from Ancient Greek: αἷμα, blood ; ποιεῖν to make ) (or hematopoiesis in the United States; sometimes also haemopoiesis or… … Wikipedia
Sickle-cell disease — This article is about the disease itself. For the genetic transmission of sickle cell disease and its carrier state, see sickle cell trait. Sickle cell disease Classification and external resources Normal and sickle shaped red blood cells ICD 10 … Wikipedia
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Haemophilia B — Classification and external resources ICD 10 D67 ICD 9 286.1 OM … Wikipedia
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