※ PTMD 2.0 database Online Browse Options
Browse result for Rh deficiency syndrome
※ introduction 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.
Reference
DiseaseOntology: Rh deficiency syndrome
Reference
DiseaseOntology: Rh deficiency syndrome
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD06141 | Q02094 | 6005 | RHAG | Ammonium transporter Rh type A | Homo sapiens |