DISEASES

Disease-gene associations mined from literature

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