Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3007495019 | Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3007753010 | CARASIL syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3007851017 | Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3009019010 | Maeda syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3009239015 | Nemoto disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3866553018 | Cerebral autosomal recessive arteriopathy with subcortical infarcts and leucoencephalopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | Is a | Cerebrovascular disease | true | Inferred relationship | Existential restriction modifier | ||
| Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Existential restriction modifier | ||
| Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | Finding site | Cerebrovascular system structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR