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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:
ORDO:178509,
GARD:10453,
168605,
parkinsonism with alveolar hypoventilation and mental depression,
OMIM:168605,
MESH:C566822

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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