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ONTOLOGY REPORT - ANNOTATIONS


Term:Familial Mixed Cryoglobulinemia
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Accession:DOID:9004792 term browser browse the term
Synonyms:exact_synonym: Meltzer Syndrome
 primary_id: MESH:C565141
 alt_id: OMIM:123550
For additional species annotation, visit the Alliance of Genome Resources.


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Familial Mixed Cryoglobulinemia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fcgr3a Fc fragment of IgG receptor IIIa JBrowse link 13 89,385,775 89,396,047 RGD:11344956

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15992
    Developmental Diseases 9280
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8094
        genetic disease 7612
          Familial Mixed Cryoglobulinemia 1
Path 2
Term Annotations click to browse term
  disease 15992
    disease of anatomical entity 15263
      Hemic and Lymphatic Diseases 1996
        hematopoietic system disease 1595
          blood coagulation disease 604
            hemorrhagic disease 591
              vascular hemostatic disease 297
                cryoglobulinemia 9
                  Familial Mixed Cryoglobulinemia 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.