|OBO ID: DOID:0060891|
|Term Name:||Parkinson's disease 19A||Search Ontology:|
|Definition:||An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. (3)|
|Ontology:||Human Disease (DOID:0060891)|
|is a type of:||
OTHER Parkinson's disease 19A PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
Your Input Welcome
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.