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ONTOLOGY REPORT - ANNOTATIONS


Term:Cowden Syndrome 7
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Accession:DOID:9001093 term browser browse the term
Synonyms:exact_synonym: CWS7
 primary_id: OMIM:616858
 alt_id: RDO:9001418
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Cowden Syndrome 7 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Sec23b Sec23 homolog B, coat complex II component JBrowse link 3 138,715,118 138,757,111 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15626
    syndrome 5163
      Multiple Hamartoma Syndrome 24
        Cowden syndrome 10
          Cowden Syndrome 7 1
Path 2
Term Annotations click to browse term
  disease 15626
    Developmental Diseases 8759
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7543
        genetic disease 7038
          monogenic disease 4659
            autosomal genetic disease 3619
              autosomal dominant disease 2135
                Cowden syndrome 10
                  Cowden Syndrome 7 1
paths to the root

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