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Term:schizophrenia 16
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Accession:DOID:0070092 term browser browse the term
Definition:A schizophrenia that has_material_basis_in a mutation on chromosome 7q36.3. (DO)
Synonyms:exact_synonym: SCZD16
 primary_id: OMIM:613959
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schizophrenia 16 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Vipr2 vasoactive intestinal peptide receptor 2 JBrowse link 6 143,932,960 144,009,476 RGD:7240710

Term paths to the root
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Term Annotations click to browse term
  disease 14924
    Developmental Diseases 7770
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7092
        genetic disease 6457
          schizophrenia 16 1
Path 2
Term Annotations click to browse term
  disease 14924
    disease of anatomical entity 14094
      nervous system disease 9141
        central nervous system disease 6931
          brain disease 6435
            disease of mental health 4324
              cognitive disorder 1834
                psychotic disorder 1076
                  schizophrenia 1007
                    schizophrenia 16 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.