Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5071675017 | Isolated hypoplasia of fovea centralis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5071676016 | Isolated foveal hypoplasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5071677013 | Isolated hypoplasia of fovea centralis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5400169010 | A rare macular disorder characterized mostly by a variable degree of decreased visual acuity, jerk or pendular nystagmus, and typical ocular findings at imaging. The disease is usually bilateral. Rarely, nystagmus can be absent. Locally, the disease is characterized by underdeveloped foveal pit, absence of foveal pigmentation and/or foveal avascular zone, and persistence of inner retinal layers at the fovea, in absence of concomitant ocular or systemic pathology. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5400170011 | A rare macular disorder characterised mostly by a variable degree of decreased visual acuity, jerk or pendular nystagmus, and typical ocular findings at imaging. The disease is usually bilateral. Rarely, nystagmus can be absent. Locally, the disease is characterised by underdeveloped foveal pit, absence of foveal pigmentation and/or foveal avascular zone, and persistence of inner retinal layers at the fovea, in absence of concomitant ocular or systemic pathology. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Isolated hypoplasia of fovea centralis (disorder) | Is a | Anomaly of eye (disorder) | true | Inferred relationship | Some | ||
| Isolated hypoplasia of fovea centralis (disorder) | Is a | Disorder of macula of retina (disorder) | true | Inferred relationship | Some | ||
| Isolated hypoplasia of fovea centralis (disorder) | Is a | Developmental disorder | true | Inferred relationship | Some | ||
| Isolated hypoplasia of fovea centralis (disorder) | Finding site | Structure of fovea centralis | true | Inferred relationship | Some | 1 | |
| Isolated hypoplasia of fovea centralis (disorder) | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
| Isolated hypoplasia of fovea centralis (disorder) | Pathological process (attribute) | Pathological developmental process | 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)
FHIR