Human genes for Rh deficiency syndrome
Rh deficiency syndrome [DOID:0050641]
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.
Synonyms: Rh deficiency syndrome, DOID:0050641, Rh deficiency disease, Rh deficiency disorder, Rh deficiency syndromes
Linkouts: OMIM