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DO Term : Parkinson's disease 19A [DOID:0060891] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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

synonyms:
OMIM:615528,
juvenile onset Parkinson's disease 19A,
615528,
juvenile onset Parkinson disease 19A,
ICD10CM:G20,
ORDO:391411

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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