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Neuroscience Information Framework (NIF) Standard Ontology
Last uploaded:
February 10, 2018
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| Id | http://purl.obolibrary.org/obo/DOID_649
http://purl.obolibrary.org/obo/DOID_649
|
|---|---|
| Preferred Name | prion disease |
| Definitions |
A brain disease that is characterized by brain damage resulting from the abnormal folding, clumping and accumulation of cellular proteins in the brain induced by prion proteins.
|
| Synonyms |
prion induced disorder
Prion protein disease
transmissible spongiform encephalopathy
Prion disease pathway
Spongiform Encephalopathy
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | A brain disease that is characterized by brain damage resulting from the abnormal folding, clumping and accumulation of cellular proteins in the brain induced by prion proteins. |
|---|---|
| preferred label |
prion disease
|
| label |
prion disease
|
| prefLabel |
prion disease
|
| database_cross_reference |
ICD10CM:A81.9
NCI:C128346
UMLS_CUI:C0162534
MESH:D017096
SNOMEDCT_US_2023_03_01:20484008
KEGG:05020
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|
| notation |
DOID:649
|
| in_subset | |
| id |
DOID:649
|
| note |
A brain disease that is characterized by brain damage resulting from the abnormal folding, clumping and accumulation of cellular proteins in the brain induced by prion proteins.
|
| alternative label |
prion induced disorder
Prion protein disease
transmissible spongiform encephalopathy
Prion disease pathway
Spongiform Encephalopathy
|
| has_obo_namespace |
disease_ontology
|
| subClassOf | |
| equivalentClass | |
| type | |
| has exact synonym |
prion induced disorder
Prion protein disease
transmissible spongiform encephalopathy
Prion disease pathway
Spongiform Encephalopathy
|
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