An instance of prion disease that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]

This is just here as a test because I lose it

Term information

database cross reference
  • ICD10:A81.8 (Orphanet:280400)
  • Orphanet:280400 (MONDO:equivalentTo)
  • UMLS:CN202725 (MONDO:equivalentTo)
Subsets

ordo_group_of_disorders

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml

definition

An instance of prion disease that is caused by an inherited modification of the individual's genome.

exactMatch

http://linkedlifedata.com/resource/umls/id/CN202725

http://www.orpha.net/ORDO/Orphanet_280400

has exact synonym

hereditary prion disease

familial prion disease

id

MONDO:0017234