Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3701687013 | Congenital Horner syndrome (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3701688015 | Congenital Horner syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3701689011 | Congenital Claude Bernard Horner syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
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 | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set