Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4553699013 | Congenital microencephaly (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4553700014 | Congenital microencephaly | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital microencephaly | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital microencephaly | Is a | Congenital anomaly of brain | true | Inferred relationship | Existential restriction modifier | ||
| Congenital microencephaly | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital microencephaly | Associated morphology | Congenital smallness | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital microencephaly | Finding site | Brain structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Microcephalic primordial dwarfism due to zinc finger protein 335 deficiency | Is a | True | Congenital microencephaly | Inferred relationship | Existential restriction modifier | |
| Reduction anomaly of hypothalamus | Is a | False | Congenital microencephaly | Inferred relationship | Existential restriction modifier | |
| Microgyria | Is a | True | Congenital microencephaly | Inferred relationship | Existential restriction modifier | |
| Microlissencephaly | Is a | True | Congenital microencephaly | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR