RADIN BLOOD GROUP ANTIGEN
General Information (adopted from Orphanet):
| Synonyms, Signs: |
BLOOD GROUP--RADIN ANTIGEN RD |
| Number of Symptoms | 1 |
| OrphanetNr: | |
| OMIM Id: |
111620
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| ICD-10: |
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| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
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| Age of onset: |
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Disease classification (adopted from Orphanet):
| Parent Diseases: | No data available. |
Symptom Information:
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(HPO:0010701) | Abnormal immunoglobulin level | 49 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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Additional Information:
| Description: (OMIM) |
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 ... |
| Molecular genetics OMIM | Wagner et al. (2003) demonstrated heterozygosity for a pro60-to-ala allele in the ERMAP gene (609017.0003) in an Rd+ proband. |