amyloid neuropathies, familial

Preferred Label : amyloid neuropathies, familial;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0026861;

UMLS CUI

C0206245;

Currated CISMeF NLP mapping
- ATTRV30M amyloidosis [ORDO Disease]
- Familial Amyloid Neuropathy [NCIt concept]
- Familial amyloid polyneuropathy [MedDRA LLT]
- Familial amyloid polyneuropathy (disorder) [SNOMED CT concept]
- Hereditary ATTR amyloidosis [ICD-11 Sub-sub category]
- Hereditary neuropathic amyloidosis [MedDRA Preferred Term]
- familial amyloid neuropathy [Disease (Nov.)]
- familial amyloid polyneuropathy, nos [SNOMED Notion]
False automatic mappings
- Amyloidosis, hereditary, transthyretin-related [OMIM Phenotype]
MeSH narrower concept(s)
- Amyloid Polyneuropathy, Iowa Type [MeSH concept]
- amyloid polyneuropathy, british type [MeSH concept]
- amyloid polyneuropathy, swiss type [MeSH concept]
- familial amyloid neuropathy, portuguese type [MeSH concept]
- familial amyloid polyneuropathy, appalachian type [MeSH concept]
- familial amyloid polyneuropathy, jewish type [MeSH concept]
- familial amyloid polyneuropathy, type IV [MeSH concept]
- familial amyloid polyneuropathy, type V [MeSH concept]
- familial amyloid polyneuropathy, type VI [MeSH concept]
Related record
- amyloid neuropathies, familial [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- ATTRV30M amyloidosis [ORDO Disease]
- Familial Amyloid Neuropathy [NCIt concept]
- Familial amyloid polyneuropathy [MedDRA LLT]
- Familial amyloid polyneuropathy (disorder) [SNOMED CT concept]
- Hereditary ATTR amyloidosis [ICD-11 Sub-sub category]
- Hereditary neuropathic amyloidosis [MedDRA Preferred Term]
- Neuropathic heredofamilial amyloidosis [ICD-10 Sub-category]
- familial amyloid neuropathy [Disease (Nov.)]
- familial amyloid polyneuropathy, nos [SNOMED Notion]

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