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Parkinson's disease 22 - Ontology Report - Rat Genome Database

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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:Parkinson's disease 22
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Accession:DOID:0080504 term browser browse the term
Definition:A late onset Parkinson's disease that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the coiled-coil-helix-coiled-coil-helix domain containing 2 gene on chromosome 7p11.2. (DO)
Synonyms:exact_synonym: CHCHD2-RELATED CONDITION;   PARK22;   Parkinson disease 22, autosomal dominant;   autosomal dominant Parkinson's disease 22
 xref: MIM:616710;   MONDO:0014742;   NCI:C205643

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Parkinson's disease 22 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 ISO ClinVar Annotator: match by term: CHCHD2-related condition | ClinVar Annotator: match by term: Parkinson disease 22, autosomal dominant OMIM
ClinVar		 PMID:23806086 PMID:24088041 PMID:25662902 PMID:25687216 PMID:25741868 More... NCBI chr12:32,464,847...32,470,871
Ensembl chr12:26,828,736...26,834,755 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19140
    Developmental Disease 14675
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 13724
        genetic disease 13391
          monogenic disease 10964
            autosomal genetic disease 10452
              autosomal dominant disease 6794
                Parkinson's disease 22 1
Path 2
Term Annotations click to browse term
  disease 19140
    disease of anatomical entity 18453
      nervous system disease 14363
        central nervous system disease 12640
          brain disease 11858
            movement disease 2631
              Parkinsonism 455
                Parkinson's disease 373
                  late onset Parkinson's disease 28
                    Parkinson's disease 22 1
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