Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4695166018 | Autosomal recessive isolated optic atrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4695167010 | Autosomal recessive isolated optic atrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4695236015 | Autosomal recessive non-syndromic optic atrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4695168017 | A rare hereditary optic atrophy characterised by an early onset of bilateral optic nerve degeneration without other systemic features. Clinical manifestations include pallor of the optic discs, severe but slowly progressing visual impairment, and in some patients also paracentral scotoma, photophobia and dyschromatopsia. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4695169013 | A rare hereditary optic atrophy characterized by an early onset of bilateral optic nerve degeneration without other systemic features. Clinical manifestations include pallor of the optic disks, severe but slowly progressing visual impairment, and in some patients also paracentral scotoma, photophobia and dyschromatopsia. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive isolated optic atrophy (disorder) | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | ||
Autosomal recessive isolated optic atrophy (disorder) | Is a | Optic atrophy of bilateral eyes (disorder) | true | Inferred relationship | Some | ||
Autosomal recessive isolated optic atrophy (disorder) | Is a | Inherited optic neuropathy | true | Inferred relationship | Some | ||
Autosomal recessive isolated optic atrophy (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Autosomal recessive isolated optic atrophy (disorder) | Finding site | Structure of left optic nerve (body structure) | true | Inferred relationship | Some | 1 | |
Autosomal recessive isolated optic atrophy (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 1 | |
Autosomal recessive isolated optic atrophy (disorder) | Finding site | Structure of right optic nerve (body structure) | true | Inferred relationship | Some | 2 | |
Autosomal recessive isolated optic atrophy (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets