Radin Blood Group Antigen; Rd

Description

Radin is a rare red cell antigen discovered by Rausen et al. (1967) in 5 families with varying ethnic backgrounds. It has been shown to cause mild to moderate hemolytic disease of the newborn in some cases. The Radin antigen is determined by a polymorphism in the ERMAP gene ({609017.0003}) and thus is a member of the blood group Scianna (Wagner et al., 2003). Radin has alternatively been labeled Sc4 to reflect this relationship.Harvey et al. (1983) estimated the frequency of the Radin antigen among Europeans to be 0.04% to 0.66% with the highest frequencies occurring among Swedes and Danes.

Clinical Features

Phenotypes and symptoms related to Radin Blood Group Antigen; Rd

  • Abnormal immunoglobulin level

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Alternative names

Radin Blood Group Antigen; Rd Is also known as blood group--radin antigen.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Radin Blood Group Antigen; Rd Recommended genes panels

Panel Name, Specifity and genes Tested/covered
ERMAP.

By Fulgent Genetics Fulgent Genetics (United States).

ERMAP
Specificity
100 %
Genes
100 %

You can get up to -7 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like THYROID DYSHORMONOGENESIS 4; TDH4