OMOP Concept 4037191
Immunoglobulin above reference range
StandardMeasurementSNOMED131136006Clinical Finding
Maps from
1
Descendants
66
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
(66)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
- 1Cyclic citrullinated peptide antibody measurement above reference range
- 1Free immunoglobulin light chain above reference range
- 1Gliadin specific immunoglobulin A antibody level increased
- 1High antibody titer
- 1Hyperimmunoglobulin E syndrome
- 1Immunosecretory disorder
- 1Raised antinuclear antibody
- 1Raised Helicobacter pylori antibody
- 1Severe dermatitis, multiple allergies, metabolic wasting syndrome
- 1Toxoplasma titer above reference range
- 2Antistreptolysin O titer above reference range
- 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
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