OMOP Concept 444407
Prion disease
StandardConditionSNOMED20484008Disorder
Maps from
6
Descendants
26
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
6 source codes normalize to Prion disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 128463 | Prion disease | Non-standard |
| ICD10CM | A81 | Atypical virus infections of central nervous system | Non-standard |
| ICD9CM | 046.7 | Other specified prion diseases of central nervous system | Non-standard |
| ICD9CM | 046.79 | Other and unspecified prion disease of central nervous system | Non-standard |
| MeSH | D017096 | Prion Diseases | Non-standard |
| Nebraska Lexicon | 20484008 | Prion disease | Non-standard |
Synonyms
Alternative names recorded for Prion disease across source vocabularies.
- encefalopatía espongiforme transmisible
- enfermedad por priones
- enfermedad por priones (trastorno)
- Prion disease (disorder)
- Transmissible spongiform encephalopathy
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(18)Roll up to these when you need a wider cohort.
- 1Degenerative brain disorder
- 1Infectious disease of brain
- 2Degenerative disease of the central nervous system
- 2Disorder of brain
- 2Infectious disease of central nervous system
- 2Infective disorder of head
- 3Degenerative disorder
- 3Disorder of head
- 3Disorder of the central nervous system
- 3Finding of brain
- 3Infectious disease
- 3Infectious disease of nervous system
- 4Central nervous system finding
- 4Disease
- 4Disorder of nervous system
- 4Head finding
- 5Clinical finding
- 5Disorder of body system
Narrower concepts
(26)Included automatically when you query with descendants.
- 1Acquired prion disease
- 1Atypical bovine spongiform encephalopathy
- 1Atypical scrapie Nor98
- 1Creutzfeldt-Jakob disease
- 1Familial Alzheimer-like prion disease
- 1Fatal familial insomnia
- 1Gerstmann-Straussler-Scheinker syndrome
- 1Prion protein systemic amyloidosis
- 1Progressive subcortical gliosis
- 1Spongiform encephalopathy
- 1Variably protease sensitive prionopathy
- 1Variant Creutzfeldt-Jakob disease
- 2Atypical bovine spongiform encephalopathy - H type
- 2Atypical bovine spongiform encephalopathy - L type
- 2Bovine spongiform encephalopathy
- 2Chronic wasting disease
- 2Familial Creutzfeldt-Jakob
- 2Iatrogenic Jakob-Creutzfeldt disease
- 2Kuru
- 2Scrapie
- 2Sporadic Creutzfeldt-Jakob disease
- 2Sporadic fatal insomnia
- 2Transmissible mink encephalopathy
- 3Classical sporadic Creutzfeldt-Jakob disease
- 3Creutzfeldt-Jakob Disease caused by human growth hormone
- 3Creutzfeldt Jakob disease following graft of dura
Get this concept via the API
Resolve Prion disease - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/444407?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card