ONTOLOGY REPORT - ANNOTATIONS


Term:Pyropoikilocytosis, Hereditary
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Accession:DOID:9000212 term browser browse the term
Synonyms:exact_synonym: HPP
 primary_id: MESH:C563004;   RDO:0012469
 alt_id: OMIM:266140
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Pyropoikilocytosis, Hereditary term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Spta1 spectrin, alpha, erythrocytic 1 JBrowse link 13 92,264,231 92,340,091 RGD:7240710
RGD:8554872
G Sptb spectrin, beta, erythrocytic JBrowse link 6 99,657,144 99,783,189 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14920
    disease of anatomical entity 14086
      hematopoietic system disease 1375
        hereditary elliptocytosis 8
          Pyropoikilocytosis, Hereditary 2
Path 2
Term Annotations click to browse term
  disease 14920
    disease of anatomical entity 14086
      Hemic and Lymphatic Diseases 1591
        hematopoietic system disease 1375
          anemia 369
            normocytic anemia 173
              hemolytic anemia 173
                congenital hemolytic anemia 123
                  hereditary elliptocytosis 8
                    Pyropoikilocytosis, Hereditary 2
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.