Rh deficiency syndrome
Information
- Disease name
- Rh deficiency syndrome
- Disease ID
- DOID:0050641
- Description
- "A hemolytic anemia that is characterized by deficiency of Rh antigens, has_material_basis_in homozygous or compound heterozygous mutation in the RHAG gene on chromosome 6p12." [url:https\://rarediseases.info.nih.gov/diseases/12916/rh-deficiency-syndrome, url:https\://www.ncbi.nlm.nih.gov/pubmed/3103426]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:583
- Cross Reference ID (Disease Ontology)
- GARD:12916
- Cross Reference ID (Disease Ontology)
- MESH:C562717
- Cross Reference ID (Disease Ontology)
- MIM:268150