Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2023. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5246529013 | Isolated aplasia of optic nerve (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5246530015 | Isolated optic nerve aplasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5246538010 | Isolated aplasia of optic nerve | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5400754019 | A rare developmental defect during embryogenesis characterized by congenital absence of the optic nerve head, optic nerve fibers, retinal ganglion cells, and retinal blood vessels in a malformed eye. It often occurs unilaterally with otherwise normal brain development. In bilateral cases it is accompanied by other central nervous system malformations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400755018 | A rare developmental defect during embryogenesis characterised by congenital absence of the optic nerve head, optic nerve fibres, retinal ganglion cells, and retinal blood vessels in a malformed eye. It often occurs unilaterally with otherwise normal brain development. In bilateral cases it is accompanied by other central nervous system malformations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5246529013 | Isolated aplasia of optic nerve (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5246530015 | Isolated optic nerve aplasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5246538010 | Isolated aplasia of optic nerve | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5246531016 | A rare developmental defect during embryogenesis characterized by congenital absence of the optic nerve head, optic nerve fibers, retinal ganglion cells and retinal blood vessels in a malformed eye. It often occurs unilaterally with otherwise normal brain development. In bilateral cases it is accompanied by other central nervous system malformations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5246532011 | A rare developmental defect during embryogenesis characterised by congenital absence of the optic nerve head, optic nerve fibres, retinal ganglion cells and retinal blood vessels in a malformed eye. It often occurs unilaterally with otherwise normal brain development. In bilateral cases it is accompanied by other central nervous system malformations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400754019 | A rare developmental defect during embryogenesis characterized by congenital absence of the optic nerve head, optic nerve fibers, retinal ganglion cells, and retinal blood vessels in a malformed eye. It often occurs unilaterally with otherwise normal brain development. In bilateral cases it is accompanied by other central nervous system malformations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400755018 | A rare developmental defect during embryogenesis characterised by congenital absence of the optic nerve head, optic nerve fibres, retinal ganglion cells, and retinal blood vessels in a malformed eye. It often occurs unilaterally with otherwise normal brain development. In bilateral cases it is accompanied by other central nervous system malformations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
567531000274118 | Isolierte Aplasie des Sehnervs | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
595401000274118 | Isolierte Sehnerv-Aplasie | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
567531000274118 | Isolierte Aplasie des Sehnervs | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
595401000274118 | Isolierte Sehnerv-Aplasie | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Isolated aplasia of optic nerve (disorder) | Is a | Aplasia of optic nerve (disorder) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Isolated aplasia of optic nerve (disorder) | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Isolated aplasia of optic nerve (disorder) | Finding site | Optic nerve structure | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Isolated aplasia of optic nerve (disorder) | Associated morphology | Aplasia | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Isolated aplasia of optic nerve (disorder) | Pathological process (attribute) | Pathological developmental process (qualifier value) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)