familial amyloid polyneuropathy, type vi

Preferred Label : familial amyloid polyneuropathy, type vi;

Origin ID

D6-94551;

UMLS CUI

C0268383;

Automatic exact mappings (from CISMeF team)
- amyloid neuropathies, familial [MeSH Descriptor]
- familial amyloid polyneuropathy, appalachian type [MeSH concept]
- familial amyloid polyneuropathy, type VI [MeSH concept]
Currated CISMeF NLP mapping
- Familial amyloid polyneuropathy, type VI (disorder) [SNOMED CT concept]
False UMLS correspondences (reviewed by CISMeF team)
- amyloid neuropathies, familial [MeSH Descriptor]
ICD-10 exact mapping(s)
- Neuropathic heredofamilial amyloidosis [ICD-10 Sub-category (who)]
Metaterm(s)
- internal medicine [CISMeF Metaterm]
- metabolism [CISMeF Metaterm]
- neurology [CISMeF Metaterm]
SNOMED CT concept
- Familial amyloid polyneuropathy, type VI (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial amyloid polyneuropathy, type VI (disorder) [SNOMED CT concept]
- familial amyloid polyneuropathy, type VI [MeSH concept]