OMOP Concept 4004635
Trisomy 13, meiotic nondisjunction
StandardConditionSNOMED205619006Disorder
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 13, meiotic nondisjunction via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 159158 | Trisomy 13, meiotic nondisjunction | Non-standard |
| CIM10 | Q91.4 | Trisomy 13, meiotic nondisjunction | Non-standard |
| ICD10 | Q91.4 | Trisomy 13, meiotic nondisjunction | Non-standard |
| ICD10CM | Q91.4 | Trisomy 13, nonmosaicism (meiotic nondisjunction) | Non-standard |
| ICD10CN | Q91.4 | Trisomy 13, meiotic nondisjunction | Non-standard |
| ICD10CN | Q91.400 | Trisomy 13, meiotic nondisjunction | Non-standard |
| ICD10GM | Q91.4 | Trisomy 13, meiotic nondisjunction | Non-standard |
| KCD7 | Q91.4 | Trisomy 13, meiotic nondisjunction | Non-standard |
| Nebraska Lexicon | 205619006 | Trisomy 13, meiotic nondisjunction | Non-standard |
| Read | PJ10.00 | Trisomy 13, meiotic nondisjunction | Non-standard |
Synonyms
Alternative names recorded for Trisomy 13, meiotic nondisjunction across source vocabularies.
- trisomía 13 - sin disyunción meiótica
- trisomía 13 - sin disyunción meiótica (trastorno)
- Trisomy 13, 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 13 syndrome
- 1Congenital malformation
- 1Whole chromosome trisomy meiotic nondisjunction
- 2Anomaly of chromosome pair 13
- 2Congenital disease
- 2Developmental disorder
- 2Trisomy and partial trisomy of autosome
- 3Anomaly of chromosome pair
- 3Autosomal duplication
- 3Congenital chromosomal disease
- 3Disease
- 3Disorder of fetus and/or newborn
- 4Autosomal chromosomal disorder
- 4Chromosomal disorder
- 4Clinical finding
- 4Duplication of chromosome
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