nvCJD - New variant of Creutzfeldt-Jakob disease

disorder

SNOMED 304603007CUI C0376329

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Elevated csf protein

Occasional (5-29%)HP:0002922

Cerebellar signs

HP:0001317

Confusion

HP:0001289

Delusions

HP:0000746

Depression

HP:0000716

Difficulty finding words

HP:0002381

Excessive, persistent worry and fear

HP:0000739

Extrapyramidal muscular rigidity

HP:0007076

Hallucinations

HP:0000738

Hemiparesis

HP:0001269

Inability to coordinate movements when walking

HP:0002066

Involuntary jerking movements

HP:0001336

Irritable mood

HP:0000737

Lack of feeling, emotion, interest

HP:0000741

Loss of facial expression

HP:0005327

Memory loss

HP:0002354

Personality changes

HP:0000751

Poor vision

HP:0000505

Progressive dementia

HP:0000726

Supranuclear gaze paralysis

HP:0000605

Related Conditions

Prion disease(parent)

Quick Facts

SNOMED CT: 304603007
UMLS CUI: C0376329
Fully Specified Name: Variant Creutzfeldt-Jakob disease (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 20

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.