OMOP Concept 4037191
Immunoglobulin above reference range
StandardMeasurementSNOMED131136006Clinical Finding
Maps from
1
Descendants
58
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Immunoglobulin above reference range via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 137590 | Increased immunoglobulin | Non-standard |
Synonyms
Alternative names recorded for Immunoglobulin above reference range across source vocabularies.
- Immunoglobulin above reference range (finding)
- Increased immunoglobulin
- inmunoglobulina aumentada
- inmunoglobulina por encima del rango de referencia
- inmunoglobulina por encima del rango de referencia (hallazgo)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(10)Roll up to these when you need a wider cohort.
Narrower concepts
(58)Included automatically when you query with descendants.
- 1Anti-canine calprotectin immunoglobulin A antibody level increased
- 1Anti-outer-membrane porin C IgA antibody level increased
- 1Bence-Jones proteinuria
- 1Free immunoglobulin light chain above reference range
- 1Gliadin specific immunoglobulin A antibody level increased
- 1Hyperimmunoglobulin E syndrome
- 1Immunosecretory disorder
- 1Severe dermatitis, multiple allergies, metabolic wasting syndrome
- 2Autosomal dominant combined immunodeficiency due to ERBIN deficiency
- 2Autosomal dominant combined immunodeficiency due to partial IL6ST deficiency
- 2Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
- 2Autosomal recessive combined immunodeficiency due to complete IL6ST deficiency
- 2Autosomal recessive combined immunodeficiency due to IL6R deficiency
- 2Autosomal recessive combined immunodeficiency due to partial IL6ST deficiency
- 2Autosomal recessive hyper-IgE syndrome due to ZNF341 deficiency
- 2CADINS disease
- 2Macroglobulinemia
- 2Monoclonal gammopathy (clinical)
- 2Netherton syndrome
- 2Persistent Bence Jones proteinuria
- 2PGM3-related congenital disorder of glycosylation
- 2Polyclonal gammopathy
- 3Benign monoclonal gammopathy
- 3Biclonal gammopathy
- 3Heavy chain disease
- 3IgM lambda monoclonal paraprotein
- 3Light chain disease
- 3Mixed cryoimmunoglobulinemia with monoclonal component
- 3Mixed polyclonal cryoimmunoglobulinemia
- 3Monoclonal gammopathy of uncertain significance
- 3Non-amyloid monoclonal immunoglobulin deposition disease
- 3POEMS syndrome
- 3Polyclonal hypergammaglobulinemia
- 3TEMPI syndrome
- 3Triclonal gammopathy
- 3Waldenström macroglobulinemia
- 4AL amyloidosis
- 4Alpha heavy chain disease (clinical)
- 4Benign paraproteinemia
- 4Gamma heavy chain disease (clinical)
- 4Heavy chain deposition disease
- 4IgA monoclonal gammopathy of uncertain significance
- 4IgD monoclonal gammopathy of uncertain significance
- 4IgG monoclonal gammopathy of uncertain significance
- 4IgM monoclonal gammopathy of uncertain significance
- 4Kappa light chain disease
- 4Lambda light chain disease
- 4Light chain deposition disease
- 4Light chain monoclonal gammopathy of uncertain significance
- 4Mu heavy chain disease
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