| alloalbuminaemia | The autosomal dominant condition of having serum albumin of a variant type that differs in mobility on electrophoresis from the usual type A; individuals are heterozygous or homozygous for one of the genes for variant albumin types, a genetic polymorphism without known clinical significance. See: inherited albumin variants. Origin: allo-+ albumin + G. Haima, blood, + -ia (05 Mar 2000) |
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