Term info
database cross reference
- UMLS:CN202725 (MONDO:equivalentTo)
- Orphanet:280400 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
definition
An instance of prion disease that is caused by an inherited modification of the individual's genome.
exactMatch
http://purl.obolibrary.org/obo/Orphanet_280400, http://linkedlifedata.com/resource/umls/id/CN202725
excluded subClassOf
http://purl.obolibrary.org/obo/MONDO_0024237, http://purl.obolibrary.org/obo/MONDO_0015547
has exact synonym
hereditary prion disease, familial prion disease
id
MONDO:0017234