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DO Term : Parkinson's disease 23 [DOID:0060896] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22.
  • synonyms:
  • ICD10CM:G20,
  • 616840,
  • OMIM:616840,
  • autosomal recessive early-onset Parkinson's disease 23,
  • autosomal recessive early-onset Parkinson disease 23
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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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