amyloidosis, familial

Preferred Label : amyloidosis, familial;

MeSH definition : Diseases in which there is a familial pattern of AMYLOIDOSIS.;

MeSH synonym : amyloidoses, familial; familial amyloidosis; familial amyloidoses; amyloidoses, hereditary; hereditary amyloidoses; hereditary amyloidosis; Amyloidosis, Hereditary;

CISMeF synonym : amyloidosis - hereditary; amyloidosis - hereditaries; amyloidosis hereditary;

MeSH hyponym : amyloidosis, hereditary;

Wikipedia link : https://en.wikipedia.org/wiki/Amyloidosis, familial;

Détails

Origin ID

D028226;

UMLS CUI

C0740340;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Familial amyloid polyneuropathy (disorder) [SNOMED CT concept]
- familial amyloid polyneuropathy, nos [SNOMED Notion]
Currated CISMeF NLP mapping
- Familial amyloidosis [MedDRA Preferred Term]
- Hereditary Amyloidosis [NCIt concept]
- Hereditary amyloidosis [ICD-11 Subcategory]
- Hereditary amyloidosis [ORDO Disease]
- Hereditary amyloidosis (disorder) [SNOMED CT concept]
- Heredofamilial amyloidosis, unspecified [ICD-10 Sub-category]
- familial amyloidosis [Disease (Nov.)]
Record concept(s)
- amyloidosis, familial [MeSH concept]
Related MeSH Supplementary Concept(s)
- Amyloidosis, Cerebroarterial, App-Related [MeSH Supplementary Concept]
- amyloidosis IX [MeSH Supplementary Concept]
- amyloidosis of gingiva and conjunctiva, with mental retardation [MeSH Supplementary Concept]
- amyloidosis, cutaneous bullous [MeSH Supplementary Concept]
- amyloidosis, familial visceral [MeSH Supplementary Concept]
- amyloidosis, primary cutaneous [MeSH Supplementary Concept]
- corneal dystrophy, gelatinous drop-like [MeSH Supplementary Concept]
- pigmentary disorder, reticulate, with systemic manifestations [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial amyloidosis [MedDRA Preferred Term]
- Hereditary Amyloidosis [NCIt concept]
- Hereditary amyloidosis (disorder) [SNOMED CT concept]
- familial amyloidosis [Disease (Nov.)]

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