OMOP Concept 4168318
Genetic disorder carrier
StandardConditionSNOMED47461006Clinical Finding
Maps from
10
Descendants
57
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
10 source codes normalize to Genetic disorder carrier via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 117840 | Genetic Carrier Status | Non-standard |
| CIEL | 117842 | Carrier of Genetic Disorder | Non-standard |
| ICD10CM | Z14 | Genetic carrier | Non-standard |
| ICD10CM | Z14.8 | Genetic carrier of other disease | Non-standard |
| ICD9CM | V83 | Genetic carrier status | Non-standard |
| ICD9CM | V83.8 | Other genetic carrier status | Non-standard |
| ICD9CM | V83.89 | Other genetic carrier status | Non-standard |
| MeSH | D006579 | Heterozygote | Non-standard |
| OXMIS | T3831 | GENETIC DISORDER CARRIER | Non-standard |
| Read | 677C.00 | Genetic disorder carrier | Non-standard |
Synonyms
Alternative names recorded for Genetic disorder carrier across source vocabularies.
- Carrier of genetic disease
- Genetic disorder carrier (finding)
- portador de un trastorno genético
- portador de un trastorno genético (hallazgo)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(2)Roll up to these when you need a wider cohort.
Narrower concepts
(57)Included automatically when you query with descendants.
- 1Antenatal screening shows carrier of significant haemoglobinopathy including sickle cell or thalassaemia
- 1Antenatal screening shows non significant carrier of sickle cell or thalassaemia
- 1Antenatal screening shows non significant haemoglobinopathy carrier
- 1Antenatal screening shows significant carrier of sickle cell or thalassaemia
- 1Carrier of Bloom syndrome
- 1Carrier of Canavan disease
- 1Carrier of Charcot-Marie-Tooth disease
- 1Carrier of chromosome translocation
- 1Carrier of classical phenylketonuria
- 1Carrier of congenital cystic kidney disease
- 1Carrier of Cowden syndrome
- 1Carrier of dihydrolipoamide dehydrogenase deficiency
- 1Carrier of familial adenomatous polyposis
- 1Carrier of familial combined hyperlipidemia
- 1Carrier of familial dysautonomia
- 1Carrier of familial hypercholesterolemia
- 1Carrier of Fanconi anemia group C
- 1Carrier of fragile X chromosome
- 1Carrier of galactosemia
- 1Carrier of Gaucher disease
- 1Carrier of genetic marker for cardiomyopathy
- 1Carrier of glycogen storage disease
- 1Carrier of hemochromatosis
- 1Carrier of hemoglobinopathy disorder
- 1Carrier of hereditary persistence of fetal haemoglobin
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