ONTOLOGY REPORT - ANNOTATIONS


Term:autosomal recessive early-onset Parkinson's disease 6
go back to main search page
Accession:DOID:0060369 term browser browse the term
Definition:A Parkinson's disease that has_material_basis_in mutations in the PINK1 gene on chromosome 1p36.12. (DO)
Synonyms:exact_synonym: PARK6;   PINK1-related parkinsonism;   Parkinson disease 6;   Parkinson's disease 6;   autosomal recessive early-onset Parkinson disease 6
 narrow_synonym: PARKINSON DISEASE 6, EARLY-ONSET;   PARKINSON DISEASE 6, LATE-ONSET, SUSCEPTIBILITY TO;   PARKINSON DISEASE, AUTOSOMAL RECESSIVE EARLY-ONSET, DIGENIC, PINK1/DJ1;   PARKINSON'S DISEASE 6, EARLY-ONSET;   PARKINSON'S DISEASE 6, LATE-ONSET, SUSCEPTIBILITY TO;   PARKINSON'S DISEASE, AUTOSOMAL RECESSIVE EARLY-ONSET, DIGENIC, PINK1/DJ1
 primary_id: MESH:C565276
 alt_id: OMIM:605909;   RDO:0011971
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 6 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mt-nd5 mitochondrially encoded NADH dehydrogenase 5 JBrowse link MT 11,736 13,565 RGD:8554872
G Mt-nd6 mitochondrially encoded NADH dehydrogenase 6 JBrowse link MT 13,543 14,061 RGD:8554872
G Mtfp1 mitochondrial fission process 1 JBrowse link 14 84,330,223 84,334,063 RGD:12880394
G Park7 Parkinsonism associated deglycase JBrowse link 5 167,982,438 168,004,724 RGD:8554872
G Pink1 PTEN induced putative kinase 1 JBrowse link 5 156,677,146 156,689,258 RGD:7240710
RGD:8554872
RGD:11554173

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14875
    Developmental Diseases 7711
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6750
        genetic disease 5997
          monogenic disease 2855
            autosomal genetic disease 2137
              autosomal recessive disease 1249
                autosomal recessive early-onset Parkinson's disease 6 5
Path 2
Term Annotations click to browse term
  disease 14875
    disease of anatomical entity 14051
      nervous system disease 9116
        central nervous system disease 6913
          brain disease 6418
            movement disease 993
              Parkinsonian Disorders 310
                Parkinson's disease 235
                  early-onset Parkinson's disease 10
                    autosomal recessive early-onset Parkinson's disease 6 5
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.