Term:familial erythrocytosis 2
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Accession:DOID:0060474 term browser browse the term
Definition:A primary polycythemia that has_material_basis_in homozygous or compound heterozygous mutation in the VHL gene (608537) on chromosome 3p25. (DO)
Synonyms:exact_synonym: Chuvash erythromatosis;   Chuvash polycythemia;   Chuvash type polycythemia;   ECYT2;   autosomal recessive benign erythrocytosis;   polycythemia, VHL-dependent
 primary_id: MESH:C563918
 alt_id: OMIM:263400;   RDO:0013044
 xref: ORDO:238557
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familial erythrocytosis 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Brk1 BRICK1 subunit of SCAR/WAVE actin nucleating complex JBrowse link 4 145,559,206 145,574,438 RGD:8554872
G Fancd2 FA complementation group D2 JBrowse link 4 145,489,869 145,551,479 RGD:8554872
G Fancd2os FANCD2 opposite strand JBrowse link 4 145,549,248 145,556,054 RGD:8554872
G Jak2 Janus kinase 2 JBrowse link 1 247,398,667 247,457,521 RGD:6483049
G Vhl von Hippel-Lindau tumor suppressor JBrowse link 4 145,580,869 145,587,835 RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14919
    disease of anatomical entity 14083
      hematopoietic system disease 1374
        polycythemia 24
          primary polycythemia 20
            familial erythrocytosis 2 5
Path 2
Term Annotations click to browse term
  disease 14919
    Developmental Diseases 7761
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7082
        genetic disease 6388
          monogenic disease 3218
            autosomal genetic disease 2156
              autosomal recessive disease 1257
                familial erythrocytosis 2 5
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.