Cryoglobulinemia, familial mixed

Preferred Label : Cryoglobulinemia, familial mixed;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Meltzer syndrome;

Inheritance : Autosomal dominant;

Prefixed ID : %123550;

Détails

Origin ID

123550;

UMLS CUI

C1852456;

Automatic exact mappings (from CISMeF team)
- Cryoglobulinaemia [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Cryoglobulinaemic vasculitis [ICD-11 Sub-sub category]
- Cryoglobulinemic vasculitis [ORDO Disease]
- Mixed cryoglobulinaemia [MedDRA LLT]
- Mixed cryoglobulinemia [PASCAL descriptor]
- Mixed cryoglobulinemia [MedDRA LLT]
- cryoglobulinemia, familial mixed [MeSH concept]
- cryoglobulinemia, familial mixed [MeSH Supplementary Concept]
HPO term(s)
- Abnormal renal physiology [HPO term]
- Abnormality of blood and blood-forming tissues [HPO term]
- Abnormality of renal physiology [HPO term]
- Anasarca [HPO term]
- Autosomal dominant inheritance [HPO term]
- Chronic kidney disease [HPO term]
- Cryoglobulinemia [HPO term]
- Elevated circulating creatinine concentration [HPO term]
- Hematuria [HPO term]
- Hypertension [HPO term]
- Proteinuria [HPO term]
ORDO concept(s)
- Cryoglobulinemic vasculitis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cryoglobulinemic vasculitis [ORDO Disease]
- cryoglobulinemia, familial mixed [MeSH Supplementary Concept]
- cryoglobulinemia, familial mixed [MeSH concept]

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

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