Prion protein systemic amyloidosis 733422008
SNOMED CT code
| SNOMED code | 733422008 | ||
|---|---|---|---|
| name | Prion protein systemic amyloidosis | ||
| status | active | ||
| date introduced | 2017-07-31 | ||
| fully specified name(s) | Prion protein systemic amyloidosis (disorder) | ||
| synonyms |
| ||
| attributes - group1 | |||
| Associated morphology | Amyloid deposition 68790008 | ||
| attributes - group2 | |||
| Associated morphology | Spongy degeneration 68245003 | ||
| Causative agent | Prion 84676004 | ||
| Finding site | Brain tissue structure 280369009 | ||
| Pathological process | Infectious process 441862004 | ||
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disease of the central nervous system 80690008 Hereditary degenerative disease of central nervous system 106018006 Prion protein systemic amyloidosis 733422008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Prion protein systemic amyloidosis 733422008 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 Prion protein systemic amyloidosis 733422008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Amyloidosis 17602002 Hereditary amyloidosis 367601000119103 Prion protein systemic amyloidosis 733422008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Systemic disease 56019007 Systemic amyloidosis 89449005 Prion protein systemic amyloidosis 733422008 | ||
| ancestors | sorted most to least specific
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| cpt crosswalks |
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