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ONTOLOGY REPORT - ANNOTATIONS


Term:Parkinson's disease 17
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Accession:DOID:0060897 term browser browse the term
Definition:A late-onset Parkinson disease that has_material_basis_in heterozygous mutation in the VPS35 gene on chromosome 16q13. (DO)
Synonyms:exact_synonym: PARK17;   Parkinson disease 17;   autosomal dominant Parkinson disease 17
 primary_id: OMIM:614203
 alt_id: RDO:9000630
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Parkinson's disease 17 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Vps35 VPS35 retromer complex component JBrowse link 19 27,464,937 27,500,636 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15619
    Developmental Diseases 8737
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7519
        genetic disease 7008
          monogenic disease 4561
            autosomal genetic disease 3515
              autosomal dominant disease 2079
                Parkinson's disease 17 1
Path 2
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      nervous system disease 10216
        central nervous system disease 8092
          brain disease 7561
            movement disease 1000
              Parkinsonian Disorders 322
                Parkinson's disease 248
                  late onset Parkinson's disease 24
                    Parkinson's disease 17 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.