Rh deficiency syndrome

Summary
Definition
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.
Super Class
hemolytic anemia
Disease Ontology
DOID:0050641
Mondo Disease Ontology
MeSH
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6005 RHAG Rh associated glycoprotein
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q02094 Ammonium transporter Rh type A

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 7, 2025