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Qu'est-ce (qui) est F-Hemoglobin - définition
F-Hemoglobin
WIKIMEDIA DISAMBIGUATION PAGE
Fecal Hb
F-hemoglobin (F-Hb) usually refers to hemoglobin in blood from rectal bleeding (fecal hemoglobin), but may also refer to Hemoglobin F (fetal hemoglobin).
Hemoglobin A
!['''A''':Normal [[red blood cell]]s are shown flowing freely in a [[blood vessel]] on the top of the diagram. The inset image shows a cross-section of a normal red blood cell with normal hemoglobin. '''B''':Demonstrates abnormal, sickled red blood cells blocking blood flow in a blood vessel ([[vaso-occlusive crisis]]). The inset image shows a cross-section of a sickle cell with sickle hemoglobin.
From:[http://www.nhlbi.nih.gov/health/health-topics/topics/sca/ http://www.nhlbi.nih.gov/]](https://commons.wikimedia.org/wiki/Special:FilePath/Sickle cell 01.jpg?width=200 "'''A''':Normal [[red blood cell]]s are shown flowing freely in a [[blood vessel]] on the top of the diagram. The inset image shows a cross-section of a normal red blood cell with normal hemoglobin. '''B''':Demonstrates abnormal, sickled red blood cells blocking blood flow in a blood vessel ([[vaso-occlusive crisis]]). The inset image shows a cross-section of a sickle cell with sickle hemoglobin.
From:[http://www.nhlbi.nih.gov/health/health-topics/topics/sca/ http://www.nhlbi.nih.gov/]")
AN INSTANCE OF DEFINED SET IN HOMO SAPIENS WITH REACTOME ID (R-HSA-2168876)
Adult hemoglobin; Hemoglobin A1; Haemoglobin A
Hemoglobin A (HbA), also known as adult hemoglobin, hemoglobin A1 or α2β2, is the most common human hemoglobin tetramer, accounting for over 97% of the total red blood cell hemoglobin. Hemoglobin is an oxygen-binding protein, found in erythrocytes, which transports oxygen from the lungs to the tissues.
Hemoglobin H disease
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
Hemoglobin H
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.
