Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4168264010 | Type 3 lissencephaly | en | Synonym | Active | Case insensitive | SNOMED CT core |
4168265011 | Type 3 lissencephaly (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Type 3 lissencephaly | Is a | Lissencephaly | true | Inferred relationship | Some | ||
Type 3 lissencephaly | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
Type 3 lissencephaly | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Type 3 lissencephaly | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Type 3 lissencephaly | Finding site | Brain structure | true | Inferred relationship | Some | 1 | |
Type 3 lissencephaly | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Type 3 lissencephaly | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Type 3 lissencephaly | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set