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DO Term : Perry syndrome [DOID:0060486] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A syndrome characterized by parkinsonism, hypoventilation, depression, and weight loss and that has_material_basis_in heterozygous mutation in the DCTN1 gene on chromosome 2p13.
  • synonyms:
  • parkinsonism with alveolar hypoventilation and mental depression,
  • MESH:C566822,
  • ORDO:178509,
  • OMIM:168605,
  • 168605,
  • GARD:10453
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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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