Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

ONTOLOGY REPORT - ANNOTATIONS


Term:striatonigral degeneration
go back to main search page
Accession:DOID:4751 term browser browse the term
Definition:A sporadic neurodegenerative disease with onset in middle-age characterized clinically by Parkinsonian features (e.g., MUSCLE RIGIDITY; HYPOKINESIA; stooped posture) and HYPOTENSION. This condition is considered a clinical variant of MULTIPLE SYSTEM ATROPHY. Pathologic features include a prominent loss of neurons in the zona compacta of the SUBSTANTIA NIGRA and PUTAMEN. (From Adams et al., Principles of Neurology, 6th ed, p1075-6)
Synonyms:exact_synonym: Striatonigral Atrophy;   striatonigral atrophies;   striatonigral degenerations
 narrow_synonym: Striatal Necrosis, Bilateral, with Dystonia
 primary_id: MESH:D020955
 alt_id: RDO:0007452
 xref: NCI:C125695;   OMIM:PS271930
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
striatonigral degeneration term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G NUP62 nucleoporin 62 JBrowse link 1 106,636,282 106,661,250 RGD:9068941
G PDE8B phosphodiesterase 8B JBrowse link 3 29,289,867 29,432,557 RGD:9068941
Striatonigral Degeneration, Childhood-Onset term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G VAC14 VAC14 component of PIKFYVE complex JBrowse link 5 76,635,931 76,737,414 RGD:7240710
RGD:9068941
Striatonigral Degeneration, Infantile term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G IL4I1 interleukin 4 induced 1 JBrowse link 1 106,636,282 106,673,438 RGD:9068941
G NUP62 nucleoporin 62 JBrowse link 1 106,636,282 106,661,250 RGD:7240710
RGD:9068941
Striatonigral Degeneration, Infantile, Mitochondrial term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G ATP6 ATP synthase F0 subunit 6 JBrowse link MT 7,964 8,644 RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12008
    syndrome 4665
      multiple system atrophy 27
        striatonigral degeneration 5
          Bilateral Striatal Necrosis with Dystonia 0
          Striatonigral Degeneration, Childhood-Onset 1
          Striatonigral Degeneration, Infantile 2
          Striatonigral Degeneration, Infantile, Mitochondrial 1
Path 2
Term Annotations click to browse term
  disease 12008
    disease of anatomical entity 11657
      nervous system disease 9346
        central nervous system disease 7527
          brain disease 7029
            movement disease 931
              multiple system atrophy 27
                striatonigral degeneration 5
                  Bilateral Striatal Necrosis with Dystonia 0
                  Striatonigral Degeneration, Childhood-Onset 1
                  Striatonigral Degeneration, Infantile 2
                  Striatonigral Degeneration, Infantile, Mitochondrial 1
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.