ONTOLOGY REPORT - ANNOTATIONS


Term:Rh deficiency syndrome
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Accession:DOID:0050641 term browser browse the term
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. (DO)
Synonyms:exact_synonym: RH-MOD SYNDROME;   RH-NULL HEMOLYTIC ANEMIA, REGULATOR TYPE;   RHN;   Rh-null disease;   Rh-null syndrome;   Rh-null, regulator type
 narrow_synonym: RHD NEGATIVE
 primary_id: MESH:C562717;   MESH:C564833
 alt_id: DOID:9006321;   OMIM:268150;   RDO:0012308;   RDO:0013661
 xref: GARD:12916
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Rh deficiency syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rhag Rh-associated glycoprotein JBrowse link 9 23,465,190 23,493,081 RGD:7240710
RGD:8554872
G Rhd Rh blood group, D antigen JBrowse link 5 153,197,416 153,232,009 RGD:8554872
G Rsrp1 arginine and serine rich protein 1 JBrowse link 5 153,260,930 153,264,669 RGD:8554872

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Path 1
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  disease 14875
    syndrome 4220
      Rh deficiency syndrome 3
Path 2
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  disease 14875
    disease of anatomical entity 14051
      Hemic and Lymphatic Diseases 1581
        hematopoietic system disease 1366
          anemia 367
            normocytic anemia 172
              hemolytic anemia 172
                Rh deficiency syndrome 3
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.