| 释义 |
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. |