Autosomal dominant Parkinson disease 4

Therapeutic area
Neurology
Rare disease
No

Definition
A late onset Parkinson disease that has material basis in heterozygous triplication of the alpha-synuclein gene (SNCA) on chromosome 4q22.
Genetic basis
Yes
Non-human condition
No
Rare disease
No
Listing at source
Listed
Condition name
Autosomal dominant Parkinson disease 4
Therapeutic area
Neurology

  • autosomal dominant Parkinson disease 4
  • autosomal dominant Parkinson disease type 4
  • PARK4
  • Parkinson disease 4, autosomal dominant

All therapeutic areas
  • Neurology
Sources for recorded values
Severity
Moderate

  • Genetic
  • Hereditary
Sources for recorded values

MONDO ID
Parent condition
MONDO:0008199

Related records

Broader conditions (14)

Trials (281)