Radin blood group antigen

Preferred Label : Radin blood group antigen;

Symbol : RD;

CISMeF acronym : RD;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Blood group--radin antigen;

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.;

Prefixed ID : #111620;

Details

Origin ID

111620;

UMLS CUI

C1862204;

Automatic exact mappings (from CISMeF team)
- GDC Residual Disease Terminology [NCIt concept]
- NELFE wt Allele [NCIt concept]
- Right Deltoid [NCIt concept]
- diabetic retinopathy [MeSH Descriptor]
- dyslexia susceptibility 1 [HGNC gene]
- negative elongation factor complex member E [HGNC gene]
- peroxisomal biogenesis factor 7 [ORDO Gene]
- peroxisomal biogenesis factor 7 [HGNC gene]
- phytanoyl-CoA 2-hydroxylase [ORDO Gene]
- phytanoyl-CoA 2-hydroxylase [HGNC gene]
- retinal dysplasia [MeSH Descriptor]
- supply and distribution [MeSH Qualifier]
- symbol withdrawn RD [HGNC gene]
False automatic mappings
- Blood group antigen Rd (substance) [SNOMED CT concept]
- Respiratory Distress Syndrome [NCIt concept]
- Revised diagnosis (contextual qualifier) (qualifier value) [SNOMED CT concept]
Genes related to phenotype
- Erythroblast membrane-associated protein [OMIM gene]
Semantic type(s)
- Body Substance [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients