Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3646035012 | Postlingual non-syndromic genetic deafness | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3646036013 | Isolated postlingual genetic deafness | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3646037016 | Postlingual non-syndromic genetic deafness (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3646038014 | A rare genetically highly heterogeneous otorhinolaryngologic disease, resulting from inner and/or middle ear or hearing nerve anomalies, with typical characteristics of progressive, bilateral, moderate to profound hearing loss (mean sensorineural hearing impairment equal to 40 dB or more for 500-1,000-and 2,000-Hz frequency tones in the better ear) which occurs after the onset of speech development and is not associated with visible external ear abnormalities or any other medical problems. Language development is not initially significantly delayed. | en | Definition | Inactive | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Postlingual non-syndromic genetic deafness | Pathological process | Pathological developmental process | false | Inferred relationship | Some | 1 | |
| Postlingual non-syndromic genetic deafness | Associated morphology | Morphologically abnormal structure | false | Inferred relationship | Some | 1 | |
| Postlingual non-syndromic genetic deafness | Is a | Congenital sensorineural hearing loss | false | Inferred relationship | Some | ||
| Postlingual non-syndromic genetic deafness | Is a | Developmental disorder | false | Inferred relationship | Some | ||
| Postlingual non-syndromic genetic deafness | Is a | Genetic disease | false | Inferred relationship | Some | ||
| Postlingual non-syndromic genetic deafness | Is a | Disorder of ear | false | Inferred relationship | Some | ||
| Postlingual non-syndromic genetic deafness | Is a | Non-syndromic genetic hearing loss | true | Inferred relationship | Some | ||
| Postlingual non-syndromic genetic deafness | Finding site | Structure of auditory system | true | Inferred relationship | Some | 2 | |
| Postlingual non-syndromic genetic deafness | Interprets | Hearing | true | Inferred relationship | Some | 1 | |
| Postlingual non-syndromic genetic deafness | Has interpretation | Decreased | true | Inferred relationship | Some | 1 | |
| Postlingual non-syndromic genetic deafness | Is a | Sensorineural hearing loss | false | Inferred relationship | Some | ||
| Postlingual non-syndromic genetic deafness | Is a | Congenital anomaly of ear with impairment of hearing | false | Inferred relationship | Some | ||
| Postlingual non-syndromic genetic deafness | Is a | Auditory system hereditary disorder | false | Inferred relationship | Some | ||
| Postlingual non-syndromic genetic deafness | Interprets | Hearing | false | Inferred relationship | Some | 2 | |
| Postlingual non-syndromic genetic deafness | Interprets | Functional observable | false | Inferred relationship | Some | ||
| Postlingual non-syndromic genetic deafness | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 1 | |
| Postlingual non-syndromic genetic deafness | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Postlingual non-syndromic genetic deafness | Finding site | Ear structure | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR