Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2023. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5159685018 | Non-syndromic genetic deafness | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 5159686017 | Non-syndromic genetic hearing loss | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 5159687014 | Non-syndromic genetic hearing loss (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 5159688016 | Isolated genetic hearing loss | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 5159689012 | Isolated genetic deafness | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Non-syndromic genetic hearing loss | Is a | Decreased hearing | true | Inferred relationship | Existential restriction modifier | ||
| Non-syndromic genetic hearing loss | Is a | Hearing loss | true | Inferred relationship | Existential restriction modifier | ||
| Non-syndromic genetic hearing loss | Is a | Genetic disease | true | Inferred relationship | Existential restriction modifier | ||
| Non-syndromic genetic hearing loss | Finding site | Structure of auditory system | true | Inferred relationship | Existential restriction modifier | 2 | |
| Non-syndromic genetic hearing loss | Interprets | Hearing, function | true | Inferred relationship | Existential restriction modifier | 1 | |
| Non-syndromic genetic hearing loss | Has interpretation | Decreased | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Postlingual non-syndromic genetic deafness | Is a | True | Non-syndromic genetic hearing loss | Inferred relationship | Existential restriction modifier | |
| Prelingual non-syndromic genetic deafness | Is a | True | Non-syndromic genetic hearing loss | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR