loading...| Preferred Name | prion disease | |
| Synonyms |
prion induced disorder Prion protein disease transmissible spongiform encephalopathy Prion disease pathway Spongiform Encephalopathy |
|
| 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. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_649 |
|
| alternative label |
prion induced disorder Prion protein disease transmissible spongiform encephalopathy Prion disease pathway Spongiform Encephalopathy |
|
| database_cross_reference |
ICD10CM:A81.9 NCI:C128346 UMLS_CUI:C0162534 MESH:D017096 SNOMEDCT_US_2023_03_01:20484008 KEGG:05020 |
|
| 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. |
|
| has exact synonym |
prion induced disorder Prion protein disease transmissible spongiform encephalopathy Prion disease pathway Spongiform Encephalopathy |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:649 |
|
| in_subset |
http://purl.obolibrary.org/obo/doid#NCIthesaurus http://purl.obolibrary.org/obo/doid#DO_infectious_disease_slim |
|
| label |
prion disease |
|
| notation |
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. |
|
| preferred label |
prion disease |
|
| prefLabel |
prion disease |
|
| subClassOf |
http://purl.obolibrary.org/obo/DOID_4 |