Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3646039018 | Isolated prelingual genetic deafness | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3646040016 | Prelingual non-syndromic genetic deafness (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3646041017 | Prelingual non-syndromic genetic deafness | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Prelingual non-syndromic genetic deafness (disorder) | Is a | Sensorineural hearing loss | false | Inferred relationship | Some | ||
| Prelingual non-syndromic genetic deafness (disorder) | Is a | Congenital anomaly of ear with impairment of hearing | false | Inferred relationship | Some | ||
| Prelingual non-syndromic genetic deafness (disorder) | Is a | Auditory system hereditary disorder | false | Inferred relationship | Some | ||
| Prelingual non-syndromic genetic deafness (disorder) | Interprets | Hearing | false | Inferred relationship | Some | 2 | |
| Prelingual non-syndromic genetic deafness (disorder) | Interprets | Functional observable | false | Inferred relationship | Some | ||
| Prelingual non-syndromic genetic deafness (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 1 | |
| Prelingual non-syndromic genetic deafness (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Prelingual non-syndromic genetic deafness (disorder) | Finding site | Ear structure | false | Inferred relationship | Some | 1 | |
| Prelingual non-syndromic genetic deafness (disorder) | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 1 | |
| Prelingual non-syndromic genetic deafness (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | false | Inferred relationship | Some | 1 | |
| Prelingual non-syndromic genetic deafness (disorder) | Is a | Congenital sensorineural hearing loss (disorder) | false | Inferred relationship | Some | ||
| Prelingual non-syndromic genetic deafness (disorder) | Is a | Genetic disease | false | Inferred relationship | Some | ||
| Prelingual non-syndromic genetic deafness (disorder) | Is a | Non-syndromic genetic hearing loss | true | Inferred relationship | Some | ||
| Prelingual non-syndromic genetic deafness (disorder) | Finding site | Structure of auditory system (body structure) | true | Inferred relationship | Some | 2 | |
| Prelingual non-syndromic genetic deafness (disorder) | Interprets | Hearing | true | Inferred relationship | Some | 1 | |
| Prelingual non-syndromic genetic deafness (disorder) | Has interpretation | Decreased | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR