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.
Farlex Partner Medical Dictionary © Farlex 2012
Rh null syn·drome(nŭl sin'drōm)
A lack of all Rh antigens, compensated hemolytic anemia, and stomatocytosis.
Medical Dictionary for the Health Professions and Nursing © Farlex 2012