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Summary Literature (0)
DOID:0060891 - Parkinson's disease 19A

Disease Ontology Definition:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31.

Synonyms: juvenile onset Parkinson disease 19A, juvenile onset Parkinson's disease 19A

Xenbase Genes : dnajc6

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014231 - juvenile onset Parkinson disease 19A

MIM:
MIM:615528 - PARKINSON DISEASE 19A, JUVENILE-ONSET; PARK19A

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), early-onset Parkinson's disease (is_a), juvenile-onset Parkinson's disease (is_a)