Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3737574015 | Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3737575019 | COL4A1-related familial vascular leukoencephalopathy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3737576018 | Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3737577010 | COL4A1-related retinal arteriolar tortuosity, infantile hemiparesis, autosomal dominant leukoencephalopathy syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3737578017 | COL4A1-related brain small vessel disease with hemorrhage | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3737579013 | COL4A1-related brain small vessel disease with haemorrhage | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3866559019 | COL4A1-related familial vascular leucoencephalopathy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3866560012 | Collagen type IV alpha 1 chain related familial vascular leucoencephalopathy | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3866561011 | COL4A1-related retinal arteriolar tortuosity, infantile hemiparesis, autosomal dominant leucoencephalopathy syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy | Is a | Intracerebral vascular finding | true | Inferred relationship | Existential restriction modifier | ||
| Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy | Is a | Leukoencephalopathy | true | Inferred relationship | Existential restriction modifier | ||
| Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy | Is a | Small vessel cerebrovascular disease | true | Inferred relationship | Existential restriction modifier | ||
| Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy | Finding site | Cerebral white matter structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy | Finding site | Intracranial vascular structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy | Is a | Disorder of blood vessel | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR