Phenotype report - sporadic (sCJD) (HGVPM3051)
Phenotype summary
GWAS Central identifier | HGVPM3051 |
---|---|
Phenotype | sporadic (sCJD) |
Used in Study | GWAS of prion diseases (HGVST1013) |
Description | Not supplied |
Variable type | Not supplied |
Variable unit | Not supplied |
Related links | Not supplied |
Phenotype annotation |
MeSH: Creutzfeldt-Jakob Syndrome (D007562) |
Phenotypes inferred from OMIM |
CREUTZFELDT-JAKOB DISEASE (123400) HPO: Supranuclear gaze palsy (HP:0000605) HPO: Depressivity (HP:0000716) HPO: Dementia (HP:0000726) HPO: Irritability (HP:0000737) HPO: Hallucinations (HP:0000738) HPO: Anxiety (HP:0000739) HPO: Apathy (HP:0000741) HPO: Delusions (HP:0000746) HPO: Personality changes (HP:0000751) HPO: Hemiparesis (HP:0001269) HPO: Confusion (HP:0001289) HPO: Myoclonus (HP:0001336) HPO: Abnormality of metabolism/homeostasis (HP:0001939) HPO: Gait ataxia (HP:0002066) HPO: Aphasia (HP:0002381) HPO: Loss of facial expression (HP:0005327) HPO: Extrapyramidal muscular rigidity (HP:0007076) |
Method details
No phenotype method details are currently available in GWAS Central.