ONTOLOGY REPORT - ANNOTATIONS


Term:Familial Erythrocytosis 6
go back to main search page
Accession:DOID:9009104 term browser browse the term
Definition:A disease characterized by an increased oxygen affinity of hemoglobin (Hb), which results in decreased delivery of oxygen into the peripheral tissues and compensatory polycythemia. Patients are generally asymptomatic, as compensatory polycythemia assures normal oxygen tissue delivery. (OMIM)
Synonyms:exact_synonym: ECYT6;   ERYTHROCYTOSIS 6;   ERYTHROCYTOSIS, BETA-GLOBIN TYPE;   POLYCYTHEMIA, BETA-GLOBIN TYPE
 primary_id: OMIM:617980
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
Familial Erythrocytosis 6 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hbb hemoglobin subunit beta JBrowse link 1 168,971,269 168,972,680 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14920
    disease of anatomical entity 14086
      hematopoietic system disease 1375
        polycythemia 24
          primary polycythemia 20
            Familial Erythrocytosis 6 1
Path 2
Term Annotations click to browse term
  disease 14920
    disease of anatomical entity 14086
      Hemic and Lymphatic Diseases 1591
        hematopoietic system disease 1375
          bone marrow disease 399
            polycythemia 24
              primary polycythemia 20
                Familial Erythrocytosis 6 1
paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.