Phenotype report - Creutzfeldt-Jakob disease (HGVPM172)
No data sets (in No Phenotypes) added to Browser
Phenotype summary
GWAS Central identifier HGVPM172
Phenotype Creutzfeldt-Jakob disease
Used in Study GWAS of Creutzfeldt-Jakob disease (HGVST122)
Description Please refer to the original paper for details
Variable type Not supplied
Variable unit Not supplied
Related links Not supplied
Phenotype annotation MeSH: Creutzfeldt-Jakob Syndrome (D007562)link
Phenotypes inferred from OMIM info CREUTZFELDT-JAKOB DISEASE (123400)link
HPO: Supranuclear gaze palsy (HP:0000605)link
HPO: Depressivity (HP:0000716)link
HPO: Dementia (HP:0000726)link
HPO: Irritability (HP:0000737)link
HPO: Hallucinations (HP:0000738)link
HPO: Anxiety (HP:0000739)link
HPO: Apathy (HP:0000741)link
HPO: Delusions (HP:0000746)link
HPO: Personality changes (HP:0000751)link
HPO: Hemiparesis (HP:0001269)link
HPO: Confusion (HP:0001289)link
HPO: Myoclonus (HP:0001336)link
HPO: Abnormality of metabolism/homeostasis (HP:0001939)link
HPO: Gait ataxia (HP:0002066)link
HPO: Aphasia (HP:0002381)link
HPO: Loss of facial expression (HP:0005327)link
HPO: Extrapyramidal muscular rigidity (HP:0007076)link
Method details
No phenotype method details are currently available in GWAS Central.