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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

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16017
    Developmental Diseases 9333
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8162
        genetic disease 7686
          monogenic disease 5443
            autosomal genetic disease 4407
              autosomal recessive disease 2386
                Parkinson's disease 7 1
Path 2
Term Annotations click to browse term
  disease 16017
    disease of anatomical entity 15271
      nervous system disease 10767
        central nervous system disease 8858
          brain disease 8145
            movement disease 1068
              Parkinsonian Disorders 325
                Parkinson's disease 252
                  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.