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 |
| 3646042012 | A rare genetically highly heterogeneous otorhinolaryngologic disease, resulting from inner and/or middle ear or hearing nerve anomalies, with typical characteristics of bilateral, severe to profound hearing loss (mean sensorineural hearing impairment of 60 dB or more for 500-1,000-, and 2,000-Hz frequency tones in the better ear) which occurs before the onset of speech development and is not associated with visible external ear abnormalities or any other medical problems. It is usually nonprogressive and impedes oral language acquisition. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4165241000052116 | prelingual icke-syndromisk ärftlig dövhet | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| 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 | true | 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 | true | Inferred relationship | Some | 2 | |
| Prelingual non-syndromic genetic deafness (disorder) | Interprets | observabel som rör funktion | false | Inferred relationship | Some | ||
| Prelingual non-syndromic genetic deafness (disorder) | Associated morphology | utvecklingsabnormitet | false | Inferred relationship | Some | 1 | |
| Prelingual non-syndromic genetic deafness (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Prelingual non-syndromic genetic deafness (disorder) | Finding site | Ear structure | true | Inferred relationship | Some | 1 | |
| Prelingual non-syndromic genetic deafness (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Prelingual non-syndromic genetic deafness (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Prelingual non-syndromic genetic deafness (disorder) | Is a | Congenital sensorineural hearing loss (disorder) | true | Inferred relationship | Some | ||
| Prelingual non-syndromic genetic deafness (disorder) | Is a | Genetic disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR