Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5048300018 | Auditory neuropathy, optic atrophy syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5048301019 | Auditory neuropathy, optic atrophy syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5399982011 | A rare mitochondrial disease characterized by bilateral auditory neuropathy and optic atrophy. Patients present hearing and visual impairment in the first or second decade of life, while psychomotor development is normal. Bilateral retinitis pigmentosa has been reported in association. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5399983018 | A rare mitochondrial disease characterised by bilateral auditory neuropathy and optic atrophy. Patients present hearing and visual impairment in the first or second decade of life, while psychomotor development is normal. Bilateral retinitis pigmentosa has been reported in association. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Auditory neuropathy, optic atrophy syndrome (disorder) | Is a | Decreased hearing (finding) | true | Inferred relationship | Some | ||
Auditory neuropathy, optic atrophy syndrome (disorder) | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | ||
Auditory neuropathy, optic atrophy syndrome (disorder) | Is a | Hearing loss associated with syndrome | true | Inferred relationship | Some | ||
Auditory neuropathy, optic atrophy syndrome (disorder) | Is a | Mitochondrial cytopathy (disorder) | true | Inferred relationship | Some | ||
Auditory neuropathy, optic atrophy syndrome (disorder) | Is a | Inherited optic neuropathy | true | Inferred relationship | Some | ||
Auditory neuropathy, optic atrophy syndrome (disorder) | Is a | Auditory system hereditary disorder | true | Inferred relationship | Some | ||
Auditory neuropathy, optic atrophy syndrome (disorder) | Is a | Optic atrophy | true | Inferred relationship | Some | ||
Auditory neuropathy, optic atrophy syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Auditory neuropathy, optic atrophy syndrome (disorder) | Finding site | Structure of auditory system (body structure) | true | Inferred relationship | Some | 3 | |
Auditory neuropathy, optic atrophy syndrome (disorder) | Interprets | Hearing | true | Inferred relationship | Some | 2 | |
Auditory neuropathy, optic atrophy syndrome (disorder) | Has interpretation | Decreased | true | Inferred relationship | Some | 2 | |
Auditory neuropathy, optic atrophy syndrome (disorder) | Finding site | Optic nerve structure | true | Inferred relationship | Some | 1 | |
Auditory neuropathy, optic atrophy syndrome (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 1 | |
Auditory neuropathy, optic atrophy syndrome (disorder) | Is a | Disorder of acoustic nerve | true | Inferred relationship | Some | ||
Auditory neuropathy, optic atrophy syndrome (disorder) | Finding site | Vestibulocochlear nerve structure | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)