Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 154722018 | Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 154723011 | Gonadal dysgenesis with sensorineural deafness, autosomal recessive inheritance | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 154724017 | Perrault syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 837205013 | Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Finding site | Structure of auditory system | true | Inferred relationship | Some | 2 | |
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Is a | Congenital sensorineural hearing loss | true | Inferred relationship | Some | ||
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Is a | Auditory system hereditary disorder | true | Inferred relationship | Some | ||
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Is a | Mitochondrial cytopathy | true | Inferred relationship | Some | ||
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Interprets | Hearing | true | Inferred relationship | Some | 3 | |
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Is a | Congenital malformation syndrome | true | Inferred relationship | Some | ||
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Associated morphology | Congenital malformation | false | Inferred relationship | Some | ||
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Is a | Multiple congenital malformations | false | Inferred relationship | Some | ||
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 1 | |
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance | Occurrence | Congenital | false | Inferred relationship | Some |
| 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