Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3324593011 | Early-onset X-linked optic atrophy (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3324594017 | Early-onset X-linked optic atrophy | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3324595016 | Non-Leber type optic atrophy with early-onset | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3324611017 | Optic atrophy type 2 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5402632016 | Early-onset X-linked optic atrophy is a rare form of hereditary optic atrophy, seen in only 4 families to date, with an onset in early childhood, characterized by progressive loss of visual acuity, significant optic nerve pallor and occasionally additional neurological manifestations, with females being unaffected. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402633014 | Early-onset X-linked optic atrophy is a rare form of hereditary optic atrophy, seen in only 4 families to date, with an onset in early childhood, characterised by progressive loss of visual acuity, significant optic nerve pallor and occasionally additional neurological manifestations, with females being unaffected. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Early-onset X-linked optic atrophy (disorder) | Is a | Hereditary optic atrophy | false | Inferred relationship | Some | ||
Early-onset X-linked optic atrophy (disorder) | Is a | X-linked hereditary disease | false | Inferred relationship | Some | ||
Early-onset X-linked optic atrophy (disorder) | Associated morphology | Primary atrophy | true | Inferred relationship | Some | 2 | |
Early-onset X-linked optic atrophy (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Early-onset X-linked optic atrophy (disorder) | Finding site | Optic nerve structure | true | Inferred relationship | Some | 2 | |
Early-onset X-linked optic atrophy (disorder) | Is a | Congenital atrophy of optic nerve (disorder) | true | Inferred relationship | Some | ||
Early-onset X-linked optic atrophy (disorder) | Is a | X-linked recessive hereditary disease | false | Inferred relationship | Some | ||
Early-onset X-linked optic atrophy (disorder) | Is a | X-linked optic atrophy | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)