Variants
Sign InSign Up

Autosomal dominant Parkinson disease 1

Your Results

Sign In

Description

Parkinson disease is the second most common neurogenic disorder after Alzheimer disease (AD; 104300), affecting approximately 1% of the population over age 50. Clinical manifestations include resting tremor, muscular rigidity, bradykinesia, and postural instability. Additional features are characteristic postural abnormalities, dysautonomia, dystonic cramps, and dementia (Polymeropoulos et al., 1996). For a general phenotypic description and a discussion of genetic heterogeneity of Parkinson disease, see 168600.

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

19

SEE THE VARIANTS →

Genes

External Links

  • OMIM

    168601

  • Orphanet
  • HPO
  • Medgen

    C1868595

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

The latest news and updates from Biocodify, sent to your inbox.