bisalbuminemia

bis·al·bu·mi·ne·mi·a

(bis'al-byū'mi-nē'mē-ă), The concurrence of having two kinds of serum albumin that differ in mobility on electrophoresis: normal albumin (albumin A) and any one of several variant types that migrate at other speeds; people are heterozygous for the gene for albumin A and the gene for the variant albumin type.
See also: inherited albumin variants.

bisalbuminemia

(bis″al-bū″mĭ-nēm′ē-ă) [ bi- + albuminemia] The presence to two distinct forms of albumin in the blood. It is a familial condition found occasionally in on protein electrophoresis, but it is not associated with disease.