A rare, genetic, parkinsonian disorder characterized by an age of onset between 21-45 years, rigidity, painful cramps followed by tremor, bradykinesia, dystonia, gait complaints and falls, and other non-motor symptoms. A slow disease progression and a more pronounced response to dopaminergic therapy are also observed in most forms of this disease.



Early-onset Parkinson disease

This is just here as a test because I lose it

Term information

database cross reference
  • https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2828
  • ICD-10:G20
  • OMIM:616840
  • OMIM:610297
  • OMIM:613643
  • OMIM:606852
  • OMIM:606324
  • OMIM:600116
  • OMIM:605909
  • OMIM:602404
  • OMIM:615528
  • OMIM:300557
has age of onset
  • http://www.orpha.net/ORDO/Orphanet_409948
has inheritance
  • http://www.orpha.net/ORDO/Orphanet_409930
has point prevalence range
  • http://www.orpha.net/ORDO/Orphanet_409975
  • ORPHA:2828
part of
  • http://www.orpha.net/ORDO/Orphanet_307055
  • http://www.orpha.net/ORDO/Orphanet_182058
  • http://www.orpha.net/ORDO/Orphanet_448426
  • http://www.orpha.net/ORDO/Orphanet_306666
present in
  • http://www.orpha.net/ORDO/Orphanet_409991
  • http://www.orpha.net/ORDO/Orphanet_409984