OBO ID: DOID:0060367
Term Name: Parkinson's disease 1 Search Ontology:
Synonyms:
  • autosomal dominant Parkinson disease 1
  • autosomal dominant Parkinson's disease 1
Definition: A late onset Parkinson's disease that has_material_basis_in mutation in the alpha-synuclein gene on chromosome 4q22.1. (2)
References:
Ontology: Human Disease   (DOID:0060367)
OTHER Parkinson's disease 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SNCA Parkinson disease 1 168601
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None