Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Mar 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4963724019 | Neuhauser Eichner Opitz syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| 4963726017 | Neuhauser Eichner Opitz syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 4964411012 | Recurrent encephalopathy of childhood | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Neuhauser Eichner Opitz syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Neuhauser Eichner Opitz syndrome | Is a | Hereditary ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Neuhauser Eichner Opitz syndrome | Finding site | Structure of nervous system | true | Inferred relationship | Existential restriction modifier | 1 | |
| Neuhauser Eichner Opitz syndrome | Is a | Chronic nervous system disorder | false | Inferred relationship | Existential restriction modifier | ||
| Neuhauser Eichner Opitz syndrome | Is a | Recurrent disease | true | Inferred relationship | Existential restriction modifier | ||
| Neuhauser Eichner Opitz syndrome | Clinical course | Recurrent | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR