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ONTOLOGY REPORT - ANNOTATIONS


Term:Parkinson's disease 7
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Accession:DOID:0060370 term browser browse the term
Definition:An early-onset Parkinson's disease that has_material_basis_in homozygous or compound heterozygous mutation in the DJ1 gene on chromosome 1p36. (DO)
Synonyms:exact_synonym: PARK7;   Parkinson disease 7;   autosomal recessive early-onset Parkinson disease 7;   autosomal recessive early-onset Parkinson's disease 7
 primary_id: MESH:C565238
 alt_id: OMIM:606324
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Parkinson's disease 7 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Park7 Parkinsonism associated deglycase JBrowse link 5 167,982,438 168,004,724 RGD:7240710
RGD:8554872
RGD:11554173

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16017
    Developmental Diseases 9307
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8132
        genetic disease 7652
          monogenic disease 5403
            autosomal genetic disease 4361
              autosomal recessive disease 2342
                Parkinson's disease 7 1
Path 2
Term Annotations click to browse term
  disease 16017
    disease of anatomical entity 15273
      nervous system disease 10762
        central nervous system disease 8856
          brain disease 8144
            movement disease 1065
              Parkinsonian Disorders 323
                Parkinson's disease 250
                  early-onset Parkinson's disease 16
                    Parkinson's disease 7 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.