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ONTOLOGY REPORT - ANNOTATIONS


Term:Parkinson's disease 21
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Accession:DOID:0111251 term browser browse the term
Definition:A late onset Parkinson's disease characterized by autosomal dominant inheritance and mean age of onset at 67 years. (DO)
Synonyms:exact_synonym: PARK21;   Parkinson disease 21
 primary_id: OMIM:616361
 alt_id: DOID:9000688;   RDO:0016169
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Parkinson's disease 21 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dnajc13 DnaJ heat shock protein family (Hsp40) member C13 JBrowse link 8 112,697,907 112,830,445 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 21 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 21 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.