Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Nov 2021. Module: SNOMED CT core module
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 | SNOMED CT core module |
| 4667452013 | HTRA1-related autosomal dominant cerebral small vessel disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 4667453015 | HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 4667454014 | HTRA1-related autosomal dominant cerebral angiopathy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease | Is a | Small vessel cerebrovascular disease | true | Inferred relationship | Existential restriction modifier | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease | Is a | Dementia | true | Inferred relationship | Existential restriction modifier | ||
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease | Finding site | Brain structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease | Finding site | Cerebrovascular system structure | true | Inferred relationship | Existential restriction modifier | 3 | |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease | Interprets | Cognitive functions | true | Inferred relationship | Existential restriction modifier | 1 | |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR