amyloid polyneuropathy, swiss type

Preferred Label : amyloid polyneuropathy, swiss type;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0335918;

UMLS CUI

C0268386;

Automatic exact mappings (from CISMeF team)
- Hereditary ATTR amyloidosis [ICD-11 Sub-sub category]
Currated CISMeF NLP mapping
- Familial amyloid polyneuropathy, type II (disorder) [SNOMED CT concept]
- familial amyloid polyneuropathy, type ii [SNOMED Notion]
Related record
- amyloid neuropathies, familial [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial amyloid polyneuropathy, type II (disorder) [SNOMED CT concept]
- familial amyloid polyneuropathy, type ii [SNOMED Notion]