OMOP Concept 4007082
Trisomy 18 - meiotic nondisjunction
StandardConditionSNOMED205623003Disorder
Maps from
10
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
10 source codes normalize to Trisomy 18 - meiotic nondisjunction via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 159161 | Trisomy 18, meiotic nondisjunction | Non-standard |
| CIM10 | Q91.0 | Trisomy 18, meiotic nondisjunction | Non-standard |
| ICD10 | Q91.0 | Trisomy 18, meiotic nondisjunction | Non-standard |
| ICD10CM | Q91.0 | Trisomy 18, nonmosaicism (meiotic nondisjunction) | Non-standard |
| ICD10CN | Q91.0 | Trisomy 18, meiotic nondisjunction | Non-standard |
| ICD10CN | Q91.000 | Trisomy 18, meiotic nondisjunction | Non-standard |
| ICD10GM | Q91.0 | Trisomy 18, meiotic nondisjunction | Non-standard |
| KCD7 | Q91.0 | Trisomy 18, meiotic nondisjunction | Non-standard |
| Nebraska Lexicon | 205623003 | Trisomy 18 - meiotic nondisjunction | Non-standard |
| Read | PJ20.00 | Trisomy 18, meiotic nondisjunction | Non-standard |
Synonyms
Alternative names recorded for Trisomy 18 - meiotic nondisjunction across source vocabularies.
- trisomía 18 - falta de disyunción meiótica
- trisomía 18 - falta de disyunción meiótica (trastorno)
- Trisomy 18 - meiotic nondisjunction (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Complete trisomy 18 syndrome
- 1Whole chromosome trisomy meiotic nondisjunction
- 2Anomaly of chromosome pair 18
- 2Congenital malformation
- 2Trisomy and partial trisomy of autosome
- 3Anomaly of chromosome pair
- 3Autosomal duplication
- 3Congenital chromosomal disease
- 3Congenital disease
- 3Developmental disorder
- 4Autosomal chromosomal disorder
- 4Chromosomal disorder
- 4Disease
- 4Disorder of fetus and/or newborn
- 4Duplication of chromosome
- 5Clinical finding
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