ONTOLOGY REPORT - ANNOTATIONS


Term:prothrombin deficiency
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Accession:DOID:2235 term browser browse the term
Definition:Absence or reduced levels of PROTHROMBIN in the blood.
Synonyms:exact_synonym: Factor II Deficiencies;   Factor II Deficiency;   Hypoprothrombinemia;   Hypoprothrombinemias;   Prothrombin Deficiencies
 primary_id: MESH:D007020;   RDO:0004116
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prothrombin deficiency term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G F2 coagulation factor II JBrowse link 3 80,529,468 80,542,993 RGD:1601108
RGD:11554173
RGD:10449425
RGD:10449424
G F7 coagulation factor VII JBrowse link 16 81,824,610 81,834,923 RGD:2312318
Prothrombin Deficiency, Congenital term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G F2 coagulation factor II JBrowse link 3 80,529,468 80,542,993 RGD:7240710
RGD:8554872
RGD:11565075

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14823
    disease of anatomical entity 13997
      hematopoietic system disease 1365
        hemorrhagic disease 376
          prothrombin deficiency 2
            Acquired Hypoprothrombinemia 0
            Prothrombin Deficiency, Congenital 1
Path 2
Term Annotations click to browse term
  disease 14823
    Developmental Diseases 7637
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6675
        genetic disease 5920
          monogenic disease 2859
            autosomal genetic disease 2140
              autosomal recessive disease 1257
                prothrombin deficiency 2
                  Acquired Hypoprothrombinemia 0
                  Prothrombin Deficiency, Congenital 1
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