OMOP Concept 4013676
Immunoglobulins outside reference range
StandardMeasurementSNOMED165939003Clinical Finding
Maps from
1
Descendants
60
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 Immunoglobulins outside reference range via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| HPO | HP_0010701 | Abnormal circulating immunoglobulin concentration | Non-standard |
Synonyms
Alternative names recorded for Immunoglobulins outside reference range across source vocabularies.
- Immunoglobulins abnormal
- Immunoglobulins outside reference range (finding)
- inmunoglobulinas anormales
- inmunoglobulinas fuera del rango de referencia
- inmunoglobulinas fuera del rango de referencia (hallazgo)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(8)Roll up to these when you need a wider cohort.
Narrower concepts
(60)Included automatically when you query with descendants.
- 1Immunoglobulin above reference range
- 1Immunoglobulin below reference range
- 2Anti-canine calprotectin immunoglobulin A antibody level increased
- 2Anti-outer-membrane porin C IgA antibody level increased
- 2Bence-Jones proteinuria
- 2Free immunoglobulin light chain above reference range
- 2Gliadin specific immunoglobulin A antibody level increased
- 2Hyperimmunoglobulin E syndrome
- 2Immunosecretory disorder
- 2Severe dermatitis, multiple allergies, metabolic wasting syndrome
- 3Autosomal dominant combined immunodeficiency due to ERBIN deficiency
- 3Autosomal dominant combined immunodeficiency due to partial IL6ST deficiency
- 3Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
- 3Autosomal recessive combined immunodeficiency due to complete IL6ST deficiency
- 3Autosomal recessive combined immunodeficiency due to IL6R deficiency
- 3Autosomal recessive combined immunodeficiency due to partial IL6ST deficiency
- 3Autosomal recessive hyper-IgE syndrome due to ZNF341 deficiency
- 3CADINS disease
- 3Macroglobulinemia
- 3Monoclonal gammopathy (clinical)
- 3Netherton syndrome
- 3Persistent Bence Jones proteinuria
- 3PGM3-related congenital disorder of glycosylation
- 3Polyclonal gammopathy
- 4Benign monoclonal gammopathy
- 4Biclonal gammopathy
- 4Heavy chain disease
- 4IgM lambda monoclonal paraprotein
- 4Light chain disease
- 4Mixed cryoimmunoglobulinemia with monoclonal component
- 4Mixed polyclonal cryoimmunoglobulinemia
- 4Monoclonal gammopathy of uncertain significance
- 4Non-amyloid monoclonal immunoglobulin deposition disease
- 4POEMS syndrome
- 4Polyclonal hypergammaglobulinemia
- 4TEMPI syndrome
- 4Triclonal gammopathy
- 4Waldenström macroglobulinemia
- 5AL amyloidosis
- 5Alpha heavy chain disease (clinical)
- 5Benign paraproteinemia
- 5Gamma heavy chain disease (clinical)
- 5Heavy chain deposition disease
- 5IgA monoclonal gammopathy of uncertain significance
- 5IgD monoclonal gammopathy of uncertain significance
- 5IgG monoclonal gammopathy of uncertain significance
- 5IgM monoclonal gammopathy of uncertain significance
- 5Kappa light chain disease
- 5Lambda light chain disease
- 5Light chain deposition disease
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