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Summary Literature (0)
DOID:0060486 - Perry syndrome

Disease Ontology Definition: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

Xenbase Genes : dctn1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008201 - Perry syndrome


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), syndrome (is_a)