Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3756877016 | Renal caliceal diverticuli and deafness syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3756879018 | Renal caliceal diverticuli and deafness syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3756878014 | A rare syndromic developmental defect during embryogenesis with characteristics of urinary tract and kidney anomalies such as renal pelvicaliceal attenuation with multiple tiny caliceal diverticula, associated with sensorineural hearing loss. There have been no further descriptions in the literature since 1981. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Renal caliceal diverticuli and deafness syndrome (disorder) | Finding site | Ear structure | true | Inferred relationship | Some | 2 | |
| Renal caliceal diverticuli and deafness syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Renal caliceal diverticuli and deafness syndrome (disorder) | Is a | Hearing loss associated with syndrome | true | Inferred relationship | Some | ||
| Renal caliceal diverticuli and deafness syndrome (disorder) | Is a | Congenital sensorineural hearing loss (disorder) | true | Inferred relationship | Some | ||
| Renal caliceal diverticuli and deafness syndrome (disorder) | Is a | Congenital anomaly of the urinary tract proper (disorder) | false | Inferred relationship | Some | ||
| Renal caliceal diverticuli and deafness syndrome (disorder) | Is a | Congenital calyceal diverticulum | true | Inferred relationship | Some | ||
| Renal caliceal diverticuli and deafness syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Renal caliceal diverticuli and deafness syndrome (disorder) | Finding site | Structure of calyx (body structure) | true | Inferred relationship | Some | 1 | |
| Renal caliceal diverticuli and deafness syndrome (disorder) | Is a | Multiple system malformation syndrome | true | Inferred relationship | Some | ||
| Renal caliceal diverticuli and deafness syndrome (disorder) | Associated morphology | Congenital diverticulum | true | Inferred relationship | Some | 1 | |
| Renal caliceal diverticuli and deafness syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Renal caliceal diverticuli and deafness syndrome (disorder) | Interprets | Hearing | true | Inferred relationship | Some | 3 | |
| Renal caliceal diverticuli and deafness syndrome (disorder) | Is a | Disorder of ear | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR