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DO Term : Parkinson's disease 8 [DOID:0060371] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A late onset Parkinson's disease that has_material_basis_in heterozygous mutation in the dardarin encoding gene on chromosome 12q12.
  • synonyms:
  • autosomal dominant Parkinson disease 8,
  • OMIM:607060,
  • autosomal dominant Parkinson's disease 8,
  • 607060
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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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