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 |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | est un(e) (attribut) | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | est un(e) (attribut) | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | est un(e) (attribut) | Small vessel cerebrovascular disease (disorder) | true | Inferred relationship | Some | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | est un(e) (attribut) | démence | true | Inferred relationship | Some | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | localisation d'une constatation (attribut) | structure de l'encéphale | true | Inferred relationship | Some | 2 | |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | localisation d'une constatation (attribut) | structure du système vasculaire cérébral | true | Inferred relationship | Some | 3 | |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | interprète (attribut) | fonctions cognitives | true | Inferred relationship | Some | 1 | |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) | a pour interprétation (attribut) | altéré | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR