Parkinson's disease 19A Disease Ontology Browser

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Parkinson's disease 19A (DOID:0060891)
Alliance: disease page
Synonyms: juvenile onset Parkinson disease 19A; juvenile onset Parkinson's disease 19A
Alt IDs: OMIM:615528, ICD10CM:G20, ORDO:391411
Definition: An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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