You are using an outdated browser. Please upgrade your browser to improve your experience.

autosomal recessive early-onset Parkinson disease 7

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any Parkinson disease in which the cause of the disease is a mutation in the PARK7 gene.
Uniprot Description A neurodegenerative disorder characterized by resting tremor, postural tremor, bradykinesia, muscular rigidity, anxiety and psychotic episodes. PARK7 has onset before 40 years, slow progression and initial good response to levodopa. Some patients may show traits reminiscent of amyotrophic lateral sclerosis-parkinsonism/dementia complex (Guam disease).
Mondo Term and Equivalent IDs
MONDO:0011658:  autosomal recessive early-onset Parkinson disease 7
MESH:C565238: 
UMLS:C1853445: