OBO ID: DOID:0060891
Term Name: Parkinson's disease 19A Search Ontology:
Synonyms:
  • juvenile onset Parkinson disease 19A
  • juvenile onset Parkinson's disease 19A
Definition: An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. (3)
References:
Ontology: Human Disease   ( DOID:0060891 )
Relationships
is a type of:
OTHER Parkinson's disease 19A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DNAJC6 Parkinson disease 19b, early-onset 615528
Parkinson disease 19a, juvenile-onset 615528
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.