hemoglobin C–thalassemia
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hemoglobin C–thalassemia disease — a hereditary disorder involving simultaneous heterozygosity for hemoglobin C and thalassemia, manifested by mild hemolytic anemia and persistent splenomegaly; called also hemoglobin C–thalassemia … Medical dictionary
hemoglobin E–thalassemia disease — a hereditary condition involving simultaneous heterozygosity for hemoglobin E and thalassemia, manifested by mild hemolytic anemia and persistent splenomegaly; called also hemoglobin E–thalassemia … Medical dictionary
hemoglobin S–thalassemia — sickle cell–thalassemia disease … Medical dictionary
hemoglobin E–thalassemia — see under disease … Medical dictionary
Thalassemia — Classification and external resources ICD 10 D56 ICD 9 282.4 … Wikipedia
hemoglobin C trait — the heterozygous state for hemoglobin C; it is asymptomatic although individuals have increased numbers of target cells in the blood. See also hemoglobin C–thalassemia disease, under disease … Medical dictionary
Hemoglobin — Hemoglobin, human, adult (heterotetramer, (αβ)2) Structure of human hemoglobin. The protein s α and β subunits are in red and blue, and the iron containing heme groups in green. Fro … Wikipedia
Hemoglobin C — (abbreviated as Hb C or HbC ) is an abnormal hemoglobin with substitution of a lysine residue for glutamic acid residue at the 6th position of the β globin chain. [ [http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 a=141900… … Wikipedia
Hemoglobin A2 — is a normal variant of hemoglobin A that consists of two alpha and two delta chains and is found in small quantity in normal human blood. Hemoglobin A2 may be increased in beta thalassemia.External links* … Wikipedia
thalassemia — [thal΄ə sē′mē ə] n. [ModL < Gr thalassa, sea + EMIA] an inherited chronic anemia, initially found among Mediterranean peoples, resulting from faulty hemoglobin production … English World dictionary
