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Human Disease

Parkinson's disease 2

Term ID
DOID:0060368
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
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Genes Involved
Zebrafish Models