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DO Term : Parkinson's disease 17 [DOID:0060897] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A late-onset Parkinson disease that has_material_basis_in heterozygous mutation in the VPS35 gene on chromosome 16q13.

synonyms:
Parkinson disease 17,
614203,
autosomal dominant Parkinson disease 17,
OMIM:614203

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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