Phenotype report - Parkinson's disease (HGVPM126)
No data sets (in No Phenotypes) added to Browser
Phenotype summary
GWAS Central identifier HGVPM126
Phenotype Parkinson's disease
Used in Study GWAS of Parkinson's disease (HGVST83)
Description Sibling pairs that are discordant for Parkinson's Disease.
Variable type Not supplied
Variable unit Not supplied
Related links Not supplied
Phenotype annotation MeSH: Parkinson Disease (D010300)link
Phenotypes inferred from OMIM info PARKINSON DISEASE (168600)link
HPO: Mask-like facies (HP:0000298)link
HPO: Depression (HP:0000716)link
HPO: Dementia (HP:0000726)link
HPO: Personality changes (HP:0000751)link
HPO: Dysarthria (HP:0001260)link
HPO: Parkinsonism (HP:0001300)link
HPO: Tremor (HP:0001337)link
HPO: Soft voice (HP:0001621)link
HPO: Rigidity (HP:0002063)link
HPO: Bradykinesia (HP:0002067)link
HPO: Hyposmia (HP:0004409)link
HPO: Short stepped shuffling gait (HP:0007311)link
Method details
No phenotype method details are currently available in GWAS Central.