Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 482126018 | Auditory system hereditary disorder | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 754765014 | Auditory system hereditary disorder (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Auditory system hereditary disorder | Is a | Disorder of auditory system | true | Inferred relationship | Some | ||
| Auditory system hereditary disorder | Is a | Hereditary disorder by system | true | Inferred relationship | Some | ||
| Auditory system hereditary disorder | Finding site | Structure of auditory system (body structure) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Epiphyseal, vertebral, ear dysplasia, nose plus associated findings syndrome (disorder) | Is a | True | Auditory system hereditary disorder | Inferred relationship | Some | |
| Infantile multisystem neurologic, endocrine, pancreatic disease (disorder) | Is a | True | Auditory system hereditary disorder | Inferred relationship | Some | |
| Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome (disorder) | Is a | True | Auditory system hereditary disorder | Inferred relationship | Some | |
| Mitchell syndrome | Is a | True | Auditory system hereditary disorder | Inferred relationship | Some | |
| Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome (disorder) | Is a | True | Auditory system hereditary disorder | Inferred relationship | Some |
This concept is not in any reference sets
FHIR