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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, X-Linked Dominant
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Accession:DOID:9006820 term browser browse the term
Synonyms:exact_synonym: Parkinson Disease, X-Linked Dominant;   X-linked dominant Parkinson disease;   X-linked dominant Parkinson's disease
 primary_id: RDO:9000400



show annotations for term's descendants           Sort by:
Parkinson's Disease, X-Linked Dominant term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G RAB39B RAB39B, member RAS oncogene family IAGP ClinVar Annotator: match by term: Parkinson disease, X-linked dominant ClinVar PMID:26399558 NCBI chr  X:155,258,235...155,264,491
Ensembl chr  X:155,258,235...155,264,491
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 35754
    Nutritional and Metabolic Diseases 10578
      disease of metabolism 10578
        Proteostasis Deficiencies 884
          synucleinopathy 455
            Parkinson's disease 415
              Parkinson's Disease, X-Linked Dominant 1
Path 2
Term Annotations click to browse term
  disease 35754
    disease of anatomical entity 32493
      nervous system disease 26373
        central nervous system disease 23608
          brain disease 22047
            movement disease 3285
              Parkinsonism 499
                Parkinson's disease 415
                  Parkinson's Disease, X-Linked Dominant 1
paths to the root