Hereditary Amyloidosis

Preferred Label : Hereditary Amyloidosis;

NCIt synonyms : Amyloidosis, Familial; AF;

NCIt related terms : Familial Amyloidosis;

NCIt definition : An autosomal dominant inherited form of amyloidosis.;

Details

Origin ID

C84555;

UMLS CUI

C0740340;

Currated CISMeF NLP mapping
- Familial amyloidosis [MedDRA Preferred Term]
- Hereditary amyloidosis [ICD-11 Subcategory]
- Hereditary amyloidosis [ORDO Disease]
- Hereditary amyloidosis (disorder) [SNOMED CT concept]
- Heredofamilial amyloidosis, unspecified [ICD-10 Sub-category]
- amyloidosis, familial [MeSH Descriptor]
- amyloidosis, familial [MeSH concept]
- familial amyloidosis [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial amyloidosis [MedDRA Preferred Term]
- Hereditary amyloidosis (disorder) [SNOMED CT concept]
- amyloidosis, familial [MeSH concept]
- amyloidosis, familial [MeSH Descriptor]
- familial amyloidosis [Disease (Nov.)]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_has_finding
- Amyloid Deposition [NCIt concept]
- Apple Green Dichromism Present in Polarized Congo-Red Stained Sections [NCIt concept]
- Hereditary Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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