ONTOLOGY REPORT - ANNOTATIONS


Term:autosomal recessive early-onset Parkinson's disease 7
go back to main search page
Accession:DOID:0060370 term browser browse the term
Definition:A 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;   autosomal recessive early-onset Parkinson disease 7
 primary_id: MESH:C565238
 alt_id: OMIM:606324;   RDO:0011969
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
autosomal recessive early-onset 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 14823
    Developmental Diseases 7637
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6675
        genetic disease 5920
          monogenic disease 2859
            autosomal genetic disease 2140
              autosomal recessive disease 1257
                autosomal recessive early-onset Parkinson's disease 7 1
Path 2
Term Annotations click to browse term
  disease 14823
    disease of anatomical entity 13997
      nervous system disease 9111
        central nervous system disease 6908
          brain disease 6412
            movement disease 991
              Parkinsonian Disorders 310
                Parkinson's disease 235
                  early-onset Parkinson's disease 10
                    autosomal recessive early-onset Parkinson's disease 7 1
paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.