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prion disease

^ http://purl.obolibrary.org/obo/DOID_649


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. [ url:http://www.hopkinsmedicine.org/healthlibrary/conditions/nervous_system_disorders/prion_diseases_134,56/ url:http://www.cdc.gov/ncidod/dvrd/prions/ url:http://en.wikipedia.org/wiki/Prion ]

Synonyms: Spongiform Encephalopathy, Prion disease pathway, prion induced disorder, Prion protein disease, transmissible spongiform encephalopathy

Term info

database cross reference
  • MESH:D017096
  • SNOMEDCT_US_2018_03_01:20484008
  • ICD10CM:A81.9
  • NCI2004_11_17:C38853
  • KEGG:05020
  • NCI:C128346
  • UMLS_CUI:C0162534
  • CSP2005:2042-5040
  • NCI2004_11_17:C27585
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DO_FlyBase_slim, NCIthesaurus

has obo namespace

disease_ontology

id

DOID:649

Term relations

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