Status: current, Primitive. Date: 30-Nov 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4667451018 | HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| 4667452013 | HTRA1-related autosomal dominant cerebral small vessel disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 4667453015 | HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 4667454014 | HTRA1-related autosomal dominant cerebral angiopathy | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 4667455010 | A rare genetic cerebral small vessel disease characterised by subcortical ischaemic events associated with cognitive decline and gait disturbance with an age of onset typically in the sixth or seventh decade of life. Imaging reveals white matter hyperintensities, status cribrosum, lacunar infarcts and sometimes microbleeds. Extra-neurological manifestations are absent. | en | Definition | Active | Case sensitive | SNOMED CT core |
| 4667456011 | A rare genetic cerebral small vessel disease characterized by subcortical ischemic events associated with cognitive decline and gait disturbance with an age of onset typically in the sixth or seventh decade of life. Imaging reveals white matter hyperintensities, status cribrosum, lacunar infarcts and sometimes microbleeds. Extra-neurological manifestations are absent. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| HTRA1-related autosomal dominant cerebral small vessel disease | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| HTRA1-related autosomal dominant cerebral small vessel disease | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
| HTRA1-related autosomal dominant cerebral small vessel disease | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| HTRA1-related autosomal dominant cerebral small vessel disease | Is a | Small vessel cerebrovascular disease | true | Inferred relationship | Some | ||
| HTRA1-related autosomal dominant cerebral small vessel disease | Is a | Dementia | true | Inferred relationship | Some | ||
| HTRA1-related autosomal dominant cerebral small vessel disease | Finding site | Brain structure | true | Inferred relationship | Some | 2 | |
| HTRA1-related autosomal dominant cerebral small vessel disease | Finding site | Cerebrovascular system structure | true | Inferred relationship | Some | 3 | |
| HTRA1-related autosomal dominant cerebral small vessel disease | Interprets | Cognitive functions | true | Inferred relationship | Some | 1 | |
| HTRA1-related autosomal dominant cerebral small vessel disease | Has interpretation | Impaired | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Mental health disorder reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set
FHIR