Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3293686019 | Congenital malformation caused by cytotoxic agents (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3297078017 | Congenital malformation caused by cytotoxic agents | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
127781000077111 | malformation congénitale causée par des agents cytotoxiques | 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 |
Congenital malformation caused by cytotoxic agents (disorder) | Is a | Congenital malformation syndromes due to known exogenous causes | false | Inferred relationship | Some | ||
Congenital malformation caused by cytotoxic agents (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
Congenital malformation caused by cytotoxic agents (disorder) | Causative agent (attribute) | médicament cytotoxique | false | Inferred relationship | Some | ||
Congenital malformation caused by cytotoxic agents (disorder) | Is a | trouble causé par un médicament | false | Inferred relationship | Some | ||
Congenital malformation caused by cytotoxic agents (disorder) | Causative agent (attribute) | Cytotoxic | false | Inferred relationship | Some | ||
Congenital malformation caused by cytotoxic agents (disorder) | Associated morphology | Congenital malformation | false | Inferred relationship | Some | ||
Congenital malformation caused by cytotoxic agents (disorder) | Is a | trouble causé par un médicament | false | Inferred relationship | Some | ||
Congenital malformation caused by cytotoxic agents (disorder) | Is a | Congenital malformation syndrome due to known exogenous cause | false | Inferred relationship | Some | ||
Congenital malformation caused by cytotoxic agents (disorder) | Is a | trouble causé par un médicament | false | Inferred relationship | Some | ||
Congenital malformation caused by cytotoxic agents (disorder) | Causative agent (attribute) | Antineoplastic agent (substance) | false | Inferred relationship | Some | ||
Congenital malformation caused by cytotoxic agents (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital malformation caused by cytotoxic agents (disorder) | Associated morphology | anomalie du développement | false | Inferred relationship | Some | 1 | |
Congenital malformation caused by cytotoxic agents (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Congenital malformation caused by cytotoxic agents (disorder) | Causative agent (attribute) | Antineoplastic agent (substance) | false | Inferred relationship | Some | 2 | |
Congenital malformation caused by cytotoxic agents (disorder) | Associated morphology | anomalie du développement | false | Inferred relationship | Some | 2 | |
Congenital malformation caused by cytotoxic agents (disorder) | Causative agent (attribute) | Antineoplastic agent (substance) | false | Inferred relationship | Some | 1 | |
Congenital malformation caused by cytotoxic agents (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital malformation caused by cytotoxic agents (disorder) | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
Congenital malformation caused by cytotoxic agents (disorder) | Is a | Congenital malformation syndrome (disorder) | true | Inferred relationship | Some | ||
Congenital malformation caused by cytotoxic agents (disorder) | Causative agent (attribute) | Cytotoxic | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Fetal aminopterin syndrome | Is a | False | Congenital malformation caused by cytotoxic agents (disorder) | Inferred relationship | Some | |
A rare teratogenic disorder due to acitretin or etretinate exposure during the first trimester of pregnancy, carrying a risk of fetal malformations of approximately 20%, including central nervous system, craniofacial, ear, thymic, cardiac and limb anomalies. | Is a | False | Congenital malformation caused by cytotoxic agents (disorder) | Inferred relationship | Some |
This concept is not in any reference sets