OBO ID: DOID:0060370
Term Name: Parkinson's disease 7 Search Ontology:
Synonyms:
  • autosomal recessive early-onset Parkinson disease 7
  • autosomal recessive early-onset Parkinson's disease 7
Definition: An early-onset Parkinson's disease that has_material_basis_in homozygous or compound heterozygous mutation in the DJ1 gene on chromosome 1p36. https://www.ncbi.nlm.nih.gov/pubmed/22315721
References:
Ontology: Human Disease   (DOID:0060370)
OTHER Parkinson's disease 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PARK7 Parkinson disease 7, autosomal recessive early-onset 606324
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None