OBO ID: DOID:0060371
Term Name: Parkinson's disease 8 Search Ontology:
Synonyms:
  • autosomal dominant Parkinson disease 8
  • autosomal dominant Parkinson's disease 8
Definition: A late onset Parkinson's disease that has_material_basis_in heterozygous mutation in the dardarin encoding gene on chromosome 12q12. https://www.ncbi.nlm.nih.gov/pubmed/22315721
References:
Ontology: Human Disease   ( DOID:0060371 )
Relationships
is a type of:
OTHER Parkinson's disease 8 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
LRRK2 {Parkinson disease 8} 607060
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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