Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2024. Module: IPS terminology module (core metadata concept)
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3701687013 | Congenital Horner syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | IPS terminology module (core metadata concept) |
| 3701688015 | Congenital Horner syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | IPS terminology module (core metadata concept) |
| 3701689011 | Congenital Claude Bernard Horner syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | IPS terminology module (core metadata concept) |
| 3701690019 | A rare neurological disorder with characteristics of relative pupillary miosis and blepharoptosis, evident at birth, caused by interruption of the oculosympathetic innervation at any point along the neural pathway from the hypothalamus to the orbit. Often additional symptoms, such as enophthalmos, facial anhidrosis, iris heterochromia, conjunctival congestion, transient hypotonia and/or pupillary dilation lag, may be present. Association with birth trauma, neoplasms or vascular malformations has been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | IPS terminology module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital Horner syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Congenital Horner syndrome (disorder) | Is a | Horner syndrome | true | Inferred relationship | Some | ||
| Congenital Horner syndrome (disorder) | Is a | Developmental disorder | true | Inferred relationship | Some | ||
| Congenital Horner syndrome (disorder) | Is a | Congenital disease | true | Inferred relationship | Some | ||
| Congenital Horner syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital Horner syndrome (disorder) | Finding site | Sympathetic nerve structure | true | Inferred relationship | Some | 1 | |
| Congenital Horner syndrome (disorder) | Pathological process (attribute) | Pathological developmental process (qualifier value) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
FHIR