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 |
| 3686396018 | Leukoencephalopathy with mild cerebellar ataxia and white matter edema | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3686397010 | CLCN2-related leukoencephalopathy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3686398017 | Leukoencephalopathy with mild cerebellar ataxia and white matter edema (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3686399013 | Leukoencephalopathy with ataxia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3686400018 | Leukoencephalopathy with mild cerebellar ataxia and white matter oedema | en | Synonym | Inactive | Entire term case insensitive | SNOMED CT core module |
| 3686401019 | CLCN2 (chloride voltage-gated channel 2) related leukoencephalopathy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3789583015 | CLCN2-related leucoencephalopathy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3789584014 | Leucoencephalopathy with mild cerebellar ataxia and white matter oedema | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3789585010 | CLCN2 (chloride voltage-gated channel 2) related leucoencephalopathy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3789586011 | Leucoencephalopathy with ataxia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Leukoencephalopathy with mild cerebellar ataxia and white matter edema | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Leukoencephalopathy with mild cerebellar ataxia and white matter edema | Is a | Leukoencephalopathy | true | Inferred relationship | Existential restriction modifier | ||
| Leukoencephalopathy with mild cerebellar ataxia and white matter edema | Finding site | Cerebellar structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Leukoencephalopathy with mild cerebellar ataxia and white matter edema | Is a | Cerebellar ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Leukoencephalopathy with mild cerebellar ataxia and white matter edema | Is a | Hereditary ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Leukoencephalopathy with mild cerebellar ataxia and white matter edema | Finding site | Cerebral white matter structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Leukoencephalopathy with mild cerebellar ataxia and white matter edema | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR