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Metadata
ID DOID:0060486
Name Perry syndrome
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.
http://www.ncbi.nlm.nih.gov/books/NBK47027/, https://ghr.nlm.nih.gov/condition/perry-syndrome
Xrefs

GARD:10453

MESH:C566822

OMIM:168605

ORDO:178509

Subsets

DO_rare_slim

Synonyms

parkinsonism with alveolar hypoventilation and mental depression [EXACT]

Parent Relationships

is_a syndrome

is_a autosomal dominant disease

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