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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

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
For additional species annotation, visit the Alliance of Genome Resources.


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schizophrenia 16 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Vipr2 vasoactive intestinal peptide receptor 2 ISO OMIM NCBI chr 6:143,932,960...144,009,476
Ensembl chr 6:143,938,040...144,008,072
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16023
    Developmental Diseases 9537
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8371
        genetic disease 7871
          monogenic disease 5714
            schizophrenia 16 1
Path 2
Term Annotations click to browse term
  disease 16023
    disease of anatomical entity 15278
      nervous system disease 10897
        central nervous system disease 9045
          brain disease 8370
            disease of mental health 6047
              cognitive disorder 1914
                psychotic disorder 1092
                  schizophrenia 1017
                    schizophrenia 16 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.