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DO Term : Parkinson's disease 2 [DOID:0060368] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An early-onset Parkinson's disease that has_material_basis_in mutation in the parkin gene on chromosome 6q25.2-q27.
  • synonyms:
  • autosomal recessive juvenile Parkinson's disease 2,
  • 600116,
  • OMIM:600116,
  • Parkinson disease juvenile type 2,
  • autosomal recessive juvenile Parkinson disease 2
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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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