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DO Term : Parkinson's disease 25 [DOID:0070486] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An early-onset Parkinson's disease characterized by mild to moderately impaired intellectual development that has_material_basis_in homozygous or compound heterozygous mutation in the PTPA gene on chromosome 9q34.11.
  • synonyms:
  • autosomal recessive early-onset Parkinson disease 25 with impaired intellectual development,
  • 620482,
  • OMIM:620482,
  • PARK25
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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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