Neuropathic heredofamilial amyloidosis

Preferred Label : Neuropathic heredofamilial amyloidosis;

Inclusion CIM-10 : Amyloid polyneuropathy (Portuguese); Transthyretin-related (ATTR) familial amyloid polyneuropathy;

Diag associé à un acte (%) : 88.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E851;

UMLS CUI

C0206245;

Currated CISMeF NLP mapping
- Familial amyloid polyneuropathy (disorder) [SNOMED CT concept]
- Hereditary ATTR amyloidosis [ICD-11 Sub-sub category]
- familial amyloid neuropathy [Disease (Nov.)]
Metaterm(s)
- genetics [CISMeF Metaterm]
Orphanet concepts
- AGel amyloidosis [ORDO Disease]
- ATTRV30M amyloidosis [ORDO Disease]
- Amyloidosis [ORDO Disease]
- Primary systemic amyloidosis [ORDO Disease]
- Variant ABeta2M amyloidosis [ORDO Disease]
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]
- amyloid neuropathies, familial [MeSH Descriptor]
- amyloid neuropathies, familial [MeSH concept]
- familial amyloid neuropathy [Disease (Nov.)]
- familial amyloid polyneuropathy, nos [SNOMED Notion]

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