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Searched for "Dystonia".

79 results found on Genetics Home Reference.

Showing results 1 to 20.
  1. dopa-responsive dystonia condition summary
    Found in name or synonym: dystonia 5, dopa-responsive type
    Related genes:
  2. task-specific focal dystonia condition summary
    Found in name or synonym: focal hand dystonia
  3. early-onset primary dystonia condition summary
    Found in name or synonym: Dystonia musculorum deformans 1
    Related genes:
  4. dystonia 6 condition summary
    Found: Dystonia 6 is one of many forms of dystonia,...
    Related genes:
  5. X-linked dystonia-parkinsonism condition summary
    Found in name or synonym: dystonia musculorum deformans
    Related genes:
  6. myoclonus-dystonia condition summary
    Found: Myoclonus-dystonia is a movement disorder that typically...
    Related genes:
  7. familial paroxysmal kinesigenic dyskinesia condition summary
    Found in name or synonym: dystonia 10
    Related genes:
  8. rapid-onset dystonia parkinsonism condition summary
    Found: Rapid-onset dystonia parkinsonism is a rare movement...
    Related genes:
  9. hypermanganesemia with dystonia, polycythemia, and cirrhosis condition summary
    Found in name or synonym: dystonia/parkinsonism, hypermanganesemia,...
    Related genes:
  10. sepiapterin reductase deficiency condition summary
    Found in name or synonym: dopa-responsive dystonia due to sepiapterin reductase deficiency
    Related genes:
  11. Partington syndrome condition summary
    Found in name or synonym: X-linked intellectual deficit-dystonia-dysarthria
    Related genes:
  12. deafness-dystonia-optic neuronopathy syndrome condition summary
    Found: Deafness-dystonia-optic neuronopathy (DDON) syndrome,...
    Related genes:
  13. dystonia definition
  14. GCH1 gene summary
    Official name: GTP cyclohydrolase 1
    Found: ...found to cause dopa-responsive dystonia. This condition is characterized...
  15. tyrosine hydroxylase deficiency condition summary
    Found: ...TH-deficient dopa-responsive dystonia (DRD). Symptoms usually appear...
    Related genes:
  16. benign essential blepharospasm condition summary
    Found: ...This condition is a type of dystonia, which is a group of movement disorders...
    Related genes:
  17. SGCE gene summary
    Official name: sarcoglycan, epsilon
    Found: ...been found to cause myoclonus-dystonia. Most of these mutations lead...
  18. TOR1A gene summary
    Official name: torsin family 1, member A (torsin A)
    Found: ...cases of early-onset primary dystonia. This mutation, which is often...
  19. TAF1 gene summary
    Official name: TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 250kDa
    Found: ...in people with X-linked dystonia-parkinsonism. Some alter single...
  20. SLC30A10 gene summary
    Official name: solute carrier family 30, member 10
    Found: ...with hypermanganesemia with dystonia, polycythemia, and cirrhosis (HMDPC)....
 
Published: April 21, 2014