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DO Term : X-linked parkinsonism-spasticity syndrome [DOID:0112105] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A movement disease characterized by slowly progressive development of parkinsonian features and variably penetrant spasticity that has_material_basis_in hemizygous mutation in the ATP6AP2 gene on chromosome Xp11.4.
  • synonyms:
  • XPDS,
  • ORDO:363654,
  • OMIM:300911,
  • X-linked Parkinsonism with spasticity,
  • 300911
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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