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Medical Term:

Rh null syndrome

 

Definition: a condition characterized by lack of all Rh antigens, compensated hemolytic anemia, and stomatocytosis; autosomal recessive inheritance, caused by mutation in the Rhesus-associated polypeptide 50-kD gene (RH50A) on chromosome 6p.

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