ONTOLOGY REPORT - ANNOTATIONS


Term:Congenital Disorder of Glycosylation Type 1X
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Accession:DOID:9002063 term browser browse the term
Synonyms:exact_synonym: CDG Ix;   CDG1X;   CDGIx;   Congenital Disorder of Glycosylation, Type Ix
 primary_id: MESH:C535751;   OMIM:615597;   RDO:9001009
 alt_id: RDO:0001040
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Congenital Disorder of Glycosylation Type 1X term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Stt3b STT3 oligosaccharyltransferase complex catalytic subunit B JBrowse link 8 123,303,910 123,370,729 RGD:7240710
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
        hemorrhagic disease 378
          blood platelet disease 193
            thrombocytopenia 129
              Congenital Disorder of Glycosylation Type 1X 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
          blood coagulation disease 392
            hemorrhagic disease 378
              blood platelet disease 193
                thrombocytopenia 129
                  Congenital Disorder of Glycosylation Type 1X 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.