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SNOMED CT code SNOMED code 20484008 name Prion disease status active date introduced 2002-01-31 fully specified name(s) Prion disease (disorder) synonyms Prion disease Transmissible spongiform encephalopathy attributes - group1 Finding site Brain structure 12738006 Pathological process Infectious process 441862004 Causative agent Prion 84676004 Associated morphology Spongy degeneration 68245003 parents children [X]Dementia in Creutzfeldt-Jakob disease 192175002 removed: 2009-01-31 Acquired prion disease 721255002 Creutzfeldt-Jakob disease 792004 Familial Alzheimer-like prion disease 721219005 Fatal familial insomnia 83157008 Gerstmann-Straussler-Scheinker syndrome 67155006 Prion protein systemic amyloidosis 733422008 Progressive subcortical gliosis 90253000 Spongiform encephalopathy 230284004 Transmissible mink encephalopathy 74286002 removed: 2014-01-31 Variably protease sensitive prionopathy 721165001 Variant Creutzfeldt-Jakob disease 304603007 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Infectious disease 40733004 Infective disorder of head 363166002 Infectious disease of brain 128614008 Prion disease 20484008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disease of the central nervous system 80690008 Degenerative brain disorder 52522001 Prion disease 20484008 ancestors sorted most to least specific
cpt crosswalks Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.
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