FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Rh deficiency syndrome ID (Ontology) DOID:0050641 (Human Disease)
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.
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 Rh deficiency syndrome       2
 for disease ribbon | Rh deficiency syndrome       2
 model of | Rh deficiency syndrome       2
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  normocytic anemia
   |__hemolytic anemia
       |__Rh deficiency syndrome  2 rec.
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GARD:12916
MESH:C562717
MIM:268150