OBO ID: DOID:0060368
Term Name: Parkinson's disease 2 Search Ontology:
Synonyms:
  • autosomal recessive juvenile Parkinson disease 2
  • autosomal recessive juvenile Parkinson's disease 2
Definition: An early-onset Parkinson's disease that has_material_basis_in mutation in the parkin gene on chromosome 6q25.2-q27. https://www.ncbi.nlm.nih.gov/pubmed/22315721
References:
Ontology: Human Disease   ( DOID:0060368 )
Relationships
is a type of:
OTHER Parkinson's disease 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PRKN Parkinson disease, juvenile, type 2 600116
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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