familial amyloid nephropathy with urticaria and deafness

Preferred Label : familial amyloid nephropathy with urticaria and deafness;

Origin ID

D6-94576;

UMLS CUI

C0268390;

Automatic exact mappings (from CISMeF team)
- cryopyrin-associated periodic syndromes [MeSH Descriptor]
Currated CISMeF NLP mapping
- Familial amyloid nephropathy with urticaria AND deafness (disorder) [SNOMED CT concept]
- Muckle-Wells Syndrome [NCIt concept]
- Muckle-Wells syndrome [MedDRA Preferred Term]
- Muckle-Wells syndrome [PASCAL descriptor]
- Muckle-Wells syndrome [ICD-11 More detail]
- Muckle-Wells syndrome [DO Concept]
- Muckle-Wells syndrome [Disease (Nov.)]
- Muckle-Wells syndrome [MeSH concept]
- Muckle-Wells syndrome [ORDO Disease]
- Muckle-wells syndrome [OMIM Phenotype]
ICD-10 exact mapping(s)
- Non-neuropathic heredofamilial amyloidosis [ICD-10 Sub-category (who)]
Metaterm(s)
- internal medicine [CISMeF Metaterm]
- metabolism [CISMeF Metaterm]
- nephrology [CISMeF Metaterm]
SNOMED CT concept
- Familial amyloid nephropathy with urticaria AND deafness (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial amyloid nephropathy with urticaria AND deafness (disorder) [SNOMED CT concept]
- Muckle-Wells Syndrome [NCIt concept]
- Muckle-Wells syndrome [ORDO Disease]
- Muckle-Wells syndrome [MeSH concept]
- Muckle-Wells syndrome [Disease (Nov.)]
- Muckle-Wells syndrome [DO Concept]
- Muckle-Wells syndrome [PASCAL descriptor]
- Muckle-Wells syndrome [ICD-11 More detail]
- Muckle-Wells syndrome [MedDRA Preferred Term]
- Muckle-wells syndrome [OMIM Phenotype]