Status: current, Primitive. Date: 31-Jan 2023. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
347699011 | Adult vitelliform macular dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
3641842010 | Adult-onset foveomacular dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
5168734011 | AOFMD - adult-onset foveomacular dystrophy | en | Synonym | Active | Case sensitive | SNOMED CT core |
5168735012 | AVMD - adult vitelliform macular dystrophy | en | Synonym | Active | Case sensitive | SNOMED CT core |
5168736013 | Gass disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
5168737016 | Pseudo-Best disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
5168738014 | Pseudo-vitelliform macular dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
5168739018 | Adult-onset vitelliform macular dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
620064010 | Adult vitelliform macular dystrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
5168733017 | A rare genetic macular dystrophy with characteristics of blurred vision, metamorphopsia and mild visual impairment secondary to a slightly elevated yellow egg yolk-like lesion located in the foveal or parafoveal region. Clinical onset is typically between the fourth and sixth decade of life. The mechanism underlying the physiopathology is unknown. An autosomal dominant inheritance with variable expression and incomplete penetrance is suggested but the disease can also be sporadic without evidence of a familial inheritance pattern. | 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
Australian dialect reference set
Problem/Diagnosis reference set