Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3303816012 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
3303817015 | Lissencephaly with cerebellar hypoplasia type D | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3303818013 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D | Is a | Lissencephaly co-occurrent with congenital cerebellar hypoplasia | true | Inferred relationship | Existential restriction modifier | ||
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D | Associated morphology | Congenital anomaly | false | Inferred relationship | Existential restriction modifier | 2 | |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D | Finding site | Brain structure | false | Inferred relationship | Existential restriction modifier | 2 | |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D | Associated morphology | Hypoplasia | false | Inferred relationship | Existential restriction modifier | 3 | |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 3 | |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D | Finding site | Cerebellar structure | false | Inferred relationship | Existential restriction modifier | 3 | |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D | Finding site | Cerebellar structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D | Associated morphology | Hypoplasia | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets