Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3656366018 | Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3656367010 | Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3656368017 | Focal epilepsy, intellectual disability, dysarthria, ataxia syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Is a | Partial seizure | true | Inferred relationship | Existential restriction modifier | ||
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Is a | Multiple system malformation syndrome | true | Inferred relationship | Existential restriction modifier | ||
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Is a | Intellectual disability | true | Inferred relationship | Existential restriction modifier | ||
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Is a | Dysgenesis of the cerebellum | true | Inferred relationship | Existential restriction modifier | ||
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Associated morphology | Developmental anomaly | false | Inferred relationship | Existential restriction modifier | 1 | |
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Finding site | Cerebellar structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Interprets | Intellectual ability | true | Inferred relationship | Existential restriction modifier | 2 | |
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 2 | |
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Interprets | Adaptation behavior | true | Inferred relationship | Existential restriction modifier | 3 | |
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR