Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4168105019 | Microlissencephaly | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4168106018 | Microlissencephaly (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4841531000052111 | mikrolissencefali | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Microlissencephaly | Is a | mikrocefali | false | Inferred relationship | Some | ||
Microlissencephaly | Is a | Lissencephaly | true | Inferred relationship | Some | ||
Microlissencephaly | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Microlissencephaly | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Microlissencephaly | Associated morphology | Congenital smallness | true | Inferred relationship | Some | 1 | |
Microlissencephaly | Finding site | Brain structure | true | Inferred relationship | Some | 1 | |
Microlissencephaly | Is a | Congenital microencephaly (disorder) | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) | Is a | True | Microlissencephaly | Inferred relationship | Some |
This concept is not in any reference sets