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