OMOP Concept 4237017
Genetic test
StandardMeasurementSNOMED405824009Procedure
Maps from
10
Descendants
305
Valid from
31 Jan 2004
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
10 source codes normalize to Genetic test via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | Z02.81 | Encounter for paternity testing | Non-standard |
| ICD10CM | Z13.7 | Encounter for screening for genetic and chromosomal anomalies | Non-standard |
| ICD10CM | Z13.79 | Encounter for other screening for genetic and chromosomal anomalies | Non-standard |
| ICD10CM | Z36.8A | Encounter for antenatal screening for other genetic defects | Non-standard |
| ICD9CM | V82.7 | Genetic screening | Non-standard |
| ICD9CM | V82.71 | Screening for genetic disease carrier status | Non-standard |
| ICD9CM | V82.79 | Other genetic screening | Non-standard |
| MeSH | D005820 | Genetic Testing | Non-standard |
| Nebraska Lexicon | 312969002 | Normal genetic findings | Non-standard |
| Nebraska Lexicon | 405824009 | Genetic test | Non-standard |
Synonyms
Alternative names recorded for Genetic test across source vocabularies.
- Genetic test (procedure)
- prueba genética
- prueba genética (procedimiento)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(5)Roll up to these when you need a wider cohort.
Narrower concepts
(305)Included automatically when you query with descendants.
- 1Gene copy number analysis
- 1Genetic screening for disorder
- 1GENETIC TEST FOR SUSCEPTIBILITY TO ORAL DISEASES (Deprecated)
- 1Human leukocyte antigen genotype determination
- 1Molecular genetic test
- 2Aldolase A fructose bisphosphate single mutation genetic test
- 2Amylo-alpha-1,6-glucosidase single mutation test
- 2Aneuploidy targeted genetic test
- 2Apolipoprotein B-100 single mutation genetic test
- 2Apolipoprotein B-100 targeted genetic test
- 2BCR-ABL gene RNA (ribonucleic acid) transcript measurement
- 2BRAF targeted genetic test
- 2BRCA1 mutation carrier detection test
- 2BRCA2 mutation carrier detection test
- 2Breakpoint cluster region c-abl oncogene 1 non-receptor tyrosine kinase targeted genetic test
- 2CALR (calreticulin) targeted genetic test
- 2Charcot-Marie-Tooth disease type 1A gene detection test
- 2Collagen, type IV, alpha 3 chain (Goodpasture antigen) comprehensive genetic test
- 2Collagen, type IV, alpha 4 chain comprehensive genetic test
- 2Collagen, type IV, alpha 5 chain comprehensive genetic test
- 2Collagen, type IV, alpha 5 chain linkage genetic test
- 2Collagen, type IV, alpha 5 chain single mutation genetic test
- 2Collagen, type VII, alpha 1 chain comprehensive genetic test
- 2Cystic fibrosis 20 common mutation test
- 2Cystic fibrosis 29 common mutation test
- 2Cystic fibrosis transmembrane conductance regulator comprehensive genetic test
- 2Cystic fibrosis transmembrane conductance regulator linkage genetic test
- 2Cystic fibrosis transmembrane conductance regulator single mutation genetic test
- 2Cystic fibrosis transmembrane conductance regulator targeted genetic test
- 2Cytochrome P450, family 2, subfamily C, polypeptide 9 targeted genetic test
- 2Cytochrome P450, family 4, subfamily F, polypeptide 2 p.Val433Met single mutation genetic test
- 2del 22q11 targeted genetic test
- 2Detection of Arg3527Gln mutation in apolipoprotein B-100 gene
- 2Detection of BCR-ABL translocation
- 2Detection of factor V Leiden mutation and prothrombin G20210A mutation
- 2Detection of mutation in apolipoprotein B-100 gene
- 2Detection of mutation in low density lipoprotein receptor gene
- 2Enolase 3 single mutation genetic test
- 2Factor II (prothrombin) G20210A mutation detection
- 2Factor II (prothrombin) G20210A mutation detection test
- 2Factor VIII mutation carrier detection test
- 2Familial hypercholesterolaemia targeted genetic test
- 2Familial hypercholesterolemia comprehensive genetic test
- 2Familial medullary thyroid carcinoma mutation carrier detection test
- 2Fragile X comprehensive genetic test
- 2Fragile X linkage genetic test
- 2Fragile X targeted genetic test
- 2Gene mutation analysis
- 2Genetic testing, comprehensive cardiac ion channel analysis, for variants in 5 major cardiac ion channel genes for individuals with high index of suspicion for familial long qt syndrome (lqts) or related syndromes (Deprecated)
- 2Genetic testing, family-specific ion channel analysis, for blood-relatives of individuals (index case) who have previously tested positive for a genetic variant of a cardiac ion channel syndrome using either one of the above test configura... (Deprecated)
Get this concept via the API
Resolve Genetic test - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/4237017?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card