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- Disease Information
- Disease Comparison
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Disease Processes ▼
- Auto Immune
- Vascular-Arteriosclerosis
- Biochemical
- Congenital-developmental
- Deficiency
- Degenrative-Necrosis
- Electromagnetic-Physics
- Eponymic
- Functional-Physiologic
- Hereditofamilial
- Iatrogenic
- Idiopathic
- Infected Organ-Abcess
- Infectious agent
- Inflammatory-Granulomatous
- Metabolic-Storage
- Neoplastic
- Poison Agent
- Poisoned Organ
- Radiation-Xray-trauma
- Mental
- Structural-Anatomic-Foreign body
- Surgical Procedure-Complication
- Trauma
- Use-age-Atrophic
- Endocrine-Vegetative
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Major Organs-Systems ▼
- Systemic
- Pediatric
- Nervous & Sensory System (Neurology)
- Cardiovascular System
- Respiratory (Pulmonary) System
- Gastro-Intestinal (Digestive) System
- Urinary System
- Dermatologic System
- Endocrine System
- Immune System
- Musculoskeletal System
- Genital Reproductive System
- Hematopoietic System (Hematology)
- Lymphatic System
- Tissue/Cells/Organelles
Disease Information for Creutzfeld-Jakob disease: Disease Mechanism & Classification
- Clinical Manifestations (89)
- Demographics & Risk Factors (10)
- Laboratory Tests (4)
- Diagnostic Test Results (32)
- Associated Diseases & Rule outs (37)
- Disease Mechanism & Classification (27)
- Treatment (5)
- Synonyms
- Definition
- External Links Related to Creutzfeld-Jakob disease
- Specific Agent
- AGENT/Difficult to sterilize/kill
- AGENT/Epizootic disease (ex)
- AGENT/Incubation years later
- AGENT/Prion transmissable disease (ex)
- AGENT/Slow CNS virus disease (ex)
- AGENT/Slow virus (ex)
- AGENT/Virus (category)
- AGENT/Transmissible spongioform encephalopathy
- Class
- CLASS/Neurologic (category)
- Pathophysiology
- Pathophysiology/Gene locus 20p12
- Pathophysiology/Gene locus 20p27-p30
- Pathophysiology/Gene locus Chromosome 20
- Pathophysiology/Gene locus Chromosome 20p
- Pathophysiology/Gene Locus Identified/OMIM database
- Pathophysiology/Gene PRNP on Chromosome 20
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Pathophysiology/Hereditary disease/Adult manifestations
- Pathophysiology/Organ transplant/infections transferred
- Pathophysiology/CNS Prion Protein Abnormality
- Pathophysiology/Codon 129 prp Gene methionine homozygous
- Pathophysiology/Chromosome gene locus 20p12-pter
- Process
- PROCESS/Autosomal dominant hereditary disease (ex).
- PROCESS/Eponymic (category)
- PROCESS/Hereditofamilial (category)
- PROCESS/INCIDENCE/Rare disease (ex)
- PROCESS/Infection/agent specific (category)
- PROCESS/Movement disorder (ex)