JSON

prion disease

Go to external page http://purl.obolibrary.org/obo/MONDO_0005429

A transmissible disease that is caused by a protein that is able to induce abnormal folding of normal cellular proteins, leading to characteristic spongiform brain changes, which are associated with neuronal loss without an inflammatory response. Such disorders have typically long incubation periods, but are then generally rapidly progressive and are uniformly fatal. [ NCIT:C128346-modified ]

Synonyms: prion protein disease spongiform encephalopathy prion induced disorder prion disease pathway

This is just here as a test because I lose it

Term information

database cross reference
  • NANDO:1200186 (https://orcid.org/0000-0003-0011-764X)
  • NCIT:C128346 (MONDO:equivalentTo)
  • EFO:0004720 (MONDO:equivalentTo)
  • MEDGEN:56445 (MONDO:equivalentTo)
  • ICD9:046.19 (MONDO:relatedTo)
  • DOID:649 (MONDO:equivalentTo)
  • SCTID:230284004 (MONDO:equivalentTo)
  • MESH:D017096 (MONDO:equivalentTo)
  • UMLS:C0162534 (MONDO:equivalentTo)
Subsets

gard_rare, otar, rare

comment

Editor note: check relationship to spongiform encephalopathy NCIT:C27585

exactMatch

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

http://linkedlifedata.com/resource/umls/id/C0162534

http://identifiers.org/medgen/56445

http://purl.obolibrary.org/obo/NCIT_C128346

http://identifiers.org/snomedct/230284004

http://identifiers.org/mesh/D017096

id

MONDO:0005429