Polyclonal hypergammaglobulinemia

Preferred Label : Polyclonal hypergammaglobulinemia;

Inclusion CIM-10 : Benign hypergammaglobulinemic purpura; Polyclonal gammopathy NOS;

Diag associé à un acte (%) : 82.1;

Autres : 2;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D890;

UMLS CUI

C0154254;

Automatic exact mappings (from CISMeF team)
- polyclonal hypergammaglobulinemia [DO Concept]
Currated CISMeF NLP mapping
- Polyclonal Hypergammaglobulinemia [NCIt concept]
- Polyclonal hypergammaglobulinaemia [MedDRA LLT]
- Polyclonal hypergammaglobulinaemia [ICD-11 Category]
- Polyclonal hypergammaglobulinaemia [ICD-10 Sub-category (who)]
- Polyclonal hypergammaglobulinemia [MedDRA LLT]
- Polyclonal hypergammaglobulinemia [ICD-9 code]
- Polyclonal hypergammaglobulinemia (disorder) [SNOMED CT concept]
DO Cross reference
- polyclonal hypergammaglobulinemia [DO Concept]
Excluded by
- Disorders of plasma-protein metabolism, not elsewhere classified [ICD-10 Sub-category]
- Purpura and other hemorrhagic conditions [ICD-10 category]
Orphanet concepts
- Polyclonal hyperviscosity syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Polyclonal Hypergammaglobulinemia [NCIt concept]
- Polyclonal hypergammaglobulinaemia [MedDRA LLT]
- Polyclonal hypergammaglobulinaemia [ICD-11 Category]
- Polyclonal hypergammaglobulinemia [MedDRA LLT]
- Polyclonal hypergammaglobulinemia [ICD-9 code]
- Polyclonal hypergammaglobulinemia (disorder) [SNOMED CT concept]
- polyclonal hypergammaglobulinemia [DO Concept]

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