OMOP Concept 4106092
Carrier of disorder
StandardObservationSNOMED29679002Clinical Finding
Maps from
1
Descendants
129
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Carrier of disorder via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | D002353 | Carrier State | Non-standard |
Synonyms
Alternative names recorded for Carrier of disorder across source vocabularies.
- Carrier
- Carrier of disease
- Carrier of disorder (finding)
- portador
- portador de enfermedad
- portador de un trastorno
- portador de un trastorno (hallazgo)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Narrower concepts
(129)Included automatically when you query with descendants.
- 1Carrier of autosomal Alport syndrome COL4A3 (collagen type IV alpha 3) gene mutation
- 1Carrier of autosomal Alport syndrome COL4A4 (collagen type IV alpha 4) gene mutation
- 1Carrier of chromosome disorder
- 1Carrier of Connexin 26 gene mutation
- 1Carrier of cystic fibrosis gene mutation
- 1Carrier of Duchenne muscular dystrophy gene mutation
- 1Carrier of fragile X gene mutation
- 1Carrier of hemochromatosis HFE gene mutation
- 1Carrier of infectious organism
- 1Carrier of medium chain acyl-coenzyme A dehydrogenase deficiency gene mutation
- 1Carrier of metabolic disorder
- 1Carrier of neurogenetic disorder
- 1Carrier of nonsyndromic deafness
- 1Carrier of sickle cell gene mutation
- 1Carrier of Tay Sachs disease gene mutation
- 1Carrier of VLCAD (very long chain acyl-coenzyme A dehydrogenase deficiency) gene mutation
- 1Carrier of X-linked Alport syndrome COL4A5 (collagen type IV alpha 5) gene mutation
- 1Carrier state, disease expressed
- 1Carrier state, disease not expressed
- 1Genetic disorder carrier
- 1Hemophilia carrier
- 1Non-significant carrier of disorder
- 1Phenylketonuria gene carrier
- 1Significant carrier of disorder
- 2Antenatal screening shows carrier of significant haemoglobinopathy including sickle cell or thalassaemia
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