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Medical Term:


Pronunciation: al′ō-al-bū′mi-nē′mē-ă


The autosomal dominant condition of having serum albumin of a variant type that differs in mobility on electrophoresis from the usual type A; affects people who are heterozygous or homozygous for one of the alleles for variant albumin types, a genetic polymorphism without known clinical significance.

[allo- + albumin + G. haima, blood, + -ia]

See Also: inherited albumin variants, under variant

© Copyright 2017 Wolters Kluwer. All Rights Reserved. Review Date: Sep 19, 2016.