Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3661467010 | Whole chromosome trisomy meiotic nondisjunction (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3661470014 | Whole chromosome trisomy meiotic nondisjunction | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5083281000241113 | trisomie du chromosome entier, non disjonction mitotique | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Whole chromosome trisomy meiotic nondisjunction (disorder) | Is a | Trisomy and partial trisomy of autosome | true | Inferred relationship | Some | ||
| Whole chromosome trisomy meiotic nondisjunction (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Whole chromosome trisomy meiotic nondisjunction (disorder) | Associated morphology | Alteration of chromosome structure | false | Inferred relationship | Some | ||
| Whole chromosome trisomy meiotic nondisjunction (disorder) | Associated morphology | anomalie congénitale | false | Inferred relationship | Some | 1 | |
| Whole chromosome trisomy meiotic nondisjunction (disorder) | Finding site | Chromosome structure | false | Inferred relationship | Some | 1 | |
| Whole chromosome trisomy meiotic nondisjunction (disorder) | Associated morphology | anomalie congénitale | false | Inferred relationship | Some | ||
| Whole chromosome trisomy meiotic nondisjunction (disorder) | Finding site | Chromosome structure | false | Inferred relationship | Some | 1 | |
| Whole chromosome trisomy meiotic nondisjunction (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Whole chromosome trisomy meiotic nondisjunction (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Whole chromosome trisomy meiotic nondisjunction (disorder) | Finding site | Chromosome structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Trisomy 21- meiotic nondisjunction | Is a | True | Whole chromosome trisomy meiotic nondisjunction (disorder) | Inferred relationship | Some | |
| Trisomy 18 - meiotic nondisjunction | Is a | True | Whole chromosome trisomy meiotic nondisjunction (disorder) | Inferred relationship | Some | |
| Trisomy 13, meiotic nondisjunction | Is a | True | Whole chromosome trisomy meiotic nondisjunction (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR