Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4667452013 | HTRA1-related autosomal dominant cerebral small vessel disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4667453015 | HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4667454014 | HTRA1-related autosomal dominant cerebral angiopathy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 12733201000172116 | maladie autosomique dominante des petits vaisseaux du cerveau liée à HtrA sérine peptidase 1 | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 12733211000172118 | angiopathie cérébrale autosomique dominante associée à HtrA1 | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 12733221000172111 | maladie autosomique dominante des petits vaisseaux cérébraux liée à HtrA sérine peptidase 1 | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 7426571000172114 | 'HtrA serine peptidase 1'-gerelateerde autosomaal dominante 'cerebral small vessel disease' | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 7426581000172112 | HTRA1-gerelateerde autosomaal dominante ziekte van kleine hersenvaten | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | Belgian module (core metadata concept) |
| 7426591000172110 | HTRA1-gerelateerde autosomaal dominante 'cerebral small vessel disease' | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | Belgian module (core metadata concept) |
| 7426601000172117 | HTRA1-gerelateerde autosomaal dominante CSVD | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | Belgian module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | Is a | Small vessel cerebrovascular disease (disorder) | true | Inferred relationship | Some | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | Is a | Dementia | true | Inferred relationship | Some | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | Finding site | Brain structure | true | Inferred relationship | Some | 2 | |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | Finding site | Cerebrovascular system structure | true | Inferred relationship | Some | 3 | |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | Interprets | Cognitive functions | true | Inferred relationship | Some | 1 | |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR