has characteristic has characteristic disease arises from feature disease has basis in feature Creutzfeldt Jacob disease movement disorder neurodegenerative disease inherited Creutzfeldt-Jakob disease https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/6671 https://github.com/monarch-initiative/mondo/issues/6877 https://www.malacards.org/card/inherited_creutzfeldt_jakob_disease SCTID:715807002 OMIM:123400 GARD:0017307 Creutzfeldt-Jakob disease, variant, resistance to hereditary Creutzfeldt Jacob disease MONDO:0007403 Orphanet:282166 MEDGEN:155837 inherited CJD icd11.foundation:607607042 NANDO:1200189 Creutzfeldt-Jakob disease UMLS:C0751254 CJD Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia. inherited inherited neurodegenerative disorder