cryoglobulinemia, familial mixed

Preferred Label : cryoglobulinemia, familial mixed;

MeSH synonym : meltzer syndrome;

Origin ID

C565141;

UMLS CUI

C1852456;

Automatic exact mappings (from CISMeF team)
- Cryoglobulinaemia [ICD-10 Sub-category (who)]
- Cryoglobulinemia [ICD-10 Sub-category]
Currated CISMeF NLP mapping
- Cryoglobulinaemic vasculitis [ICD-11 Sub-sub category]
- Cryoglobulinemia, familial mixed [OMIM Phenotype]
- Cryoglobulinemic vasculitis [ORDO Disease]
- Mixed cryoglobulinaemia [MedDRA LLT]
- Mixed cryoglobulinemia [MedDRA LLT]
- Mixed cryoglobulinemia [PASCAL descriptor]
MeSH term(s) associated for indexing
- cryoglobulinemia [MeSH Descriptor]
- genetic diseases, inborn [MeSH Descriptor]
Record concept(s)
- cryoglobulinemia, familial mixed [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cryoglobulinemia, familial mixed [OMIM Phenotype]
- Cryoglobulinemic vasculitis [ORDO Disease]