Status: current, Sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 4591809015 | Familial porencephaly (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module | 
| 4591810013 | Familial porencephalic cyst | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 4591811012 | Familial porencephaly | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values | 
| Familial porencephaly | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Familial porencephaly | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Familial porencephaly | Is a | Porencephalic cyst | true | Inferred relationship | Existential restriction modifier | ||
| Familial porencephaly | Finding site | Cerebral hemisphere structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Familial porencephaly | Associated morphology | Cyst | true | Inferred relationship | Existential restriction modifier | 1 | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
This concept is not in any reference sets