Familial amyloid polyneuropathy 42295001
SNOMED CT code
| SNOMED code | 42295001 |
|---|---|
| name | Familial amyloid polyneuropathy |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Familial amyloid polyneuropathy (disorder) |
| synonyms |
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| attributes - group1 | |
| Finding site | Peripheral nerve structure 84782009 |
| Associated morphology | Amyloid deposition 68790008 |
| parents | |
| children |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Familial amyloid polyneuropathy 42295001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Familial disease 111941005 Familial amyloid polyneuropathy 42295001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Amyloidosis 17602002 Hereditary amyloidosis 367601000119103 Familial amyloid polyneuropathy 42295001 SNOMED CT Concept 138875005 Clinical finding 404684003 General finding of soft tissue 248402002 Disorder of soft tissue 19660004 Peripheral nerve disease 302226006 Polyneuropathy 42345000 Familial amyloid polyneuropathy 42295001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Hereditary peripheral neuropathy 65017003 Familial amyloid polyneuropathy 42295001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Systemic disease 56019007 Systemic amyloidosis 89449005 Familial amyloid polyneuropathy 42295001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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