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

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

Term info

database cross reference
  • NCI:C27585
  • SNOMEDCT_US_2016_03_01:20484008
  • KEGG:05020
  • ICD10CM:A81.9
  • SNOMEDCT_US_2016_03_01:230284004
  • SNOMEDCT_US_2016_03_01:193172009
  • MESH:D017096
  • UMLS_CUI:C0162534
Subsets

DO_FlyBase_slim

has obo namespace

disease_ontology

id

DOID:649

Term relations

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