ONTOLOGY REPORT - ANNOTATIONS


Term:autosomal recessive early-onset Parkinson's disease 15
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Accession:DOID:0060372 term browser browse the term
Definition:A Parkinson's disease that has_material_basis_in mutation in the FBXO7 gene on chromosome 22q12.3. (DO)
Synonyms:exact_synonym: PARK15;   PKPS;   Pallido-Pyramidal Syndrome;   Pallidopyramidal Syndrome;   Parkinson Disease 15, Autosomal Recessive;   Parkinson's disease 15, autosomal recessive;   autosomal recessive early-onset Parkinson disease 15;   pallido-pyramidal disease;   parkinsonian-pyramidal syndrome
 primary_id: MESH:C538104
 alt_id: OMIM:260300;   RDO:0004036
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autosomal recessive early-onset Parkinson's disease 15 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fbxo7 F-box protein 7 JBrowse link 7 23,815,246 23,843,505 RGD:7240710
RGD:8554872
RGD:11554173

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Term Annotations click to browse term
  disease 14919
    syndrome 4713
      autosomal recessive early-onset Parkinson's disease 15 1
Path 2
Term Annotations click to browse term
  disease 14919
    disease of anatomical entity 14083
      nervous system disease 9147
        central nervous system disease 6945
          brain disease 6451
            movement disease 1005
              Dyskinesias 717
                dystonia 80
                  focal dystonia 10
                    blepharospasm 2
                      autosomal recessive early-onset Parkinson's disease 15 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.