Hereditary late-onset Parkinson disease

Go to external page http://www.orpha.net/ORDO/Orphanet_411602


Hereditary late-onset Parkinson disease (LOPD) is a form of Parkinson disease (PD), characterized by an age of onset of more than 50 years, tremor at rest, gait complaints and falls, bradykinesia, rigidity and painful cramps. Patients usually present a low risk of developing non motor symptoms, dystonia, dyskinesia and levodopa-induced dyskinesia (LID).

Synonyms:

LOPD

Autosomal dominant late-onset Parkinson disease

This is just here as a test because I lose it

Term information

expertlink
  • https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=411602
hasDbXref
  • OMIM:607060
  • ICD-10:G20
  • OMIM:607688
  • OMIM:605543
  • OMIM:614203
  • OMIM:616361
  • OMIM:168601
  • OMIM:614251
has age of onset
  • http://www.orpha.net/ORDO/Orphanet_409949
  • http://www.orpha.net/ORDO/Orphanet_409948
has inheritance
  • http://www.orpha.net/ORDO/Orphanet_409929
has point prevalence range
  • http://www.orpha.net/ORDO/Orphanet_409981
notation
  • ORPHA:411602
part of
  • http://www.orpha.net/ORDO/Orphanet_98534
  • http://www.orpha.net/ORDO/Orphanet_307055
  • http://www.orpha.net/ORDO/Orphanet_276058
  • 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