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