OBO ID: DOID:0060896
Term Name: Parkinson's disease 23 Search Ontology:
Synonyms:
  • autosomal recessive early-onset Parkinson disease 23
  • autosomal recessive early-onset Parkinson's disease 23
Definition: An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22. https://www.ncbi.nlm.nih.gov/pubmed/26942284
References:
Ontology: Human Disease   (DOID:0060896)
OTHER Parkinson's disease 23 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
VPS13C Parkinson disease 23, autosomal recessive, early onset 616840
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None