Familial renal amyloidosis

Preferred Label : Familial renal amyloidosis;

ICD-11 definition : This is a form of amyloidosis primarily presenting in the kidney. It is associated with fibrinogen alpha chain, apolipoprotein A1, and lysozyme.;

Détails

Origin ID

2100467097;

UMLS CUI

C0268389;

Currated CISMeF NLP mapping
- Amyloidosis, familial visceral [MeSH concept]
- Amyloidosis, hereditary systemic 2 [OMIM Phenotype]
- Familial visceral amyloidosis, Ostertag type (disorder) [SNOMED CT concept]
- Hereditary amyloidosis with primary renal involvement [ORDO Disease]
- amyloidosis, familial visceral [MeSH Supplementary Concept]
- familial visceral amyloidosis [DO Concept]
- familial visceral amyloidosis, ostertag type [SNOMED Notion]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Amyloidosis, familial visceral [MeSH concept]
- Amyloidosis, hereditary systemic 2 [OMIM Phenotype]
- Familial visceral amyloidosis, Ostertag type (disorder) [SNOMED CT concept]
- Hereditary amyloidosis with primary renal involvement [ORDO Disease]
- amyloidosis, familial visceral [MeSH Supplementary Concept]
- familial visceral amyloidosis [DO Concept]
- familial visceral amyloidosis, ostertag type [SNOMED Notion]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients