Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3309090013 | Autosomal dominant optic atrophy classic form (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3309091012 | Autosomal dominant optic atrophy classic form | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3309092017 | Autosomal dominant optic atrophy Kjer type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3309093010 | Kjer optic atrophy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3309094016 | Optic atrophy type 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401567011 | A rare neuro-ophthalmological disease which is one of the most common forms of hereditary optic neuropathy characterized by progressive bilateral visual loss with an onset during the first decade of life, associated with optic disc pallor, visual acuity loss, visual field deficits and color vision defects. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401568018 | A rare neuro-ophthalmological disease which is one of the most common forms of hereditary optic neuropathy characterised by progressive bilateral visual loss with an onset during the first decade of life, associated with optic disc pallor, visual acuity loss, visual field deficits and colour vision defects. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant optic atrophy classic form (disorder) | Is a | Dominant hereditary optic atrophy | true | Inferred relationship | Some | ||
Autosomal dominant optic atrophy classic form (disorder) | Associated morphology | Primary atrophy | true | Inferred relationship | Some | 1 | |
Autosomal dominant optic atrophy classic form (disorder) | Finding site | Optic nerve structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)