Rh null syndrome

Rh null syn·drome

[MIM*268150]
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.

Rh null syn·drome

(nŭl sin'drōm)
A lack of all Rh antigens, compensated hemolytic anemia, and stomatocytosis.