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ONTOLOGY REPORT - ANNOTATIONS


Term:secondary Parkinson disease
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Accession:DOID:13548 term browser browse the term
Definition:Conditions which feature clinical manifestations resembling primary Parkinson's disease that are caused by a known or suspected condition. Examples include parkinsonism caused by vascular injury, drugs, trauma, toxin exposure, neoplasms, infections and degenerative or hereditary conditions. Clinical features may include bradykinesia, rigidity, parkinsonian gait, and masked facies. In general, tremor is less prominent in secondary parkinsonism than in the primary form. (From Joynt, Clinical Neurology, 1998, Ch38, pp39-42)
Synonyms:exact_synonym: Secondary Parkinsonism;   Secondary Vascular Parkinson Disease;   Secondary Vascular Parkinson's Disease;   Symptomatic Parkinson Disease;   Symptomatic Parkinsonism;   atherosclerotic parkinsonism;   disorder presenting primarily with parkinsonism;   secondary Parkinson's disease;   symptomatic Parkinson's disease
 primary_id: MESH:D010302
 alt_id: RDO:0004013
 xref: NCI:C34899
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secondary Parkinson disease term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abcb1a ATP binding cassette subfamily B member 1A JBrowse link 4 22,339,829 22,517,642 RGD:11554173
G Atp13a2 ATPase cation transporting 13A2 JBrowse link 5 159,512,208 159,531,631 RGD:11554173
G Bche butyrylcholinesterase JBrowse link 2 171,104,476 171,196,186 RGD:11554173
G Cnr2 cannabinoid receptor 2 JBrowse link 5 154,242,010 154,268,126 RGD:11554173
G Fmc1 formation of mitochondrial complex V assembly factor 1 JBrowse link 4 66,276,835 66,284,868 RGD:11554173
G Gdnf glial cell derived neurotrophic factor JBrowse link 2 56,884,181 56,912,964 RGD:11554173
G Nos2 nitric oxide synthase 2 JBrowse link 10 66,188,290 66,221,621 RGD:11554173
G Pon1 paraoxonase 1 JBrowse link 4 30,249,749 30,276,297 RGD:11554173
G Prkn parkin RBR E3 ubiquitin protein ligase JBrowse link 1 48,880,015 50,069,998 RGD:11554173
G Rgs2 regulator of G-protein signaling 2 JBrowse link 13 60,846,458 60,849,061 RGD:11554173
G Shh sonic hedgehog signaling molecule JBrowse link 4 718,538 727,691 RGD:11554173
G Tfam transcription factor A, mitochondrial JBrowse link 20 18,594,057 18,606,106 RGD:11554173
MPTP Poisoning term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ins2 insulin 2 JBrowse link 1 215,856,967 215,858,034 RGD:11554173
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

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15590
    disease of anatomical entity 14919
      nervous system disease 10196
        neurodegenerative disease 2689
          secondary Parkinson disease 14
            Charcot-Marie-Tooth Disease with Ptosis and Parkinsonism 0
            MPTP Poisoning 1
            Parkinson's disease 15 1
            postencephalitic Parkinson disease 0
Path 2
Term Annotations click to browse term
  disease 15590
    disease of anatomical entity 14919
      nervous system disease 10196
        central nervous system disease 8075
          brain disease 7543
            movement disease 999
              Parkinsonian Disorders 322
                secondary Parkinson disease 14
                  Charcot-Marie-Tooth Disease with Ptosis and Parkinsonism 0
                  MPTP Poisoning 1
                  Parkinson's disease 15 1
                  postencephalitic Parkinson disease 0
paths to the root

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