773771008: Rare isolated myopia (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Eye / vision finding\Visual system disorder\...
• \Hereditary disorder of the visual system\Rare isolated myopia
• \Disorder of vision\Disorder of refraction AND/OR accommodation\Disorder of refraction\Myopia\Severe myopia\Rare isolated myopia
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the visual system\Rare isolated myopia
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Rare isolated myopia
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the visual system\Rare isolated myopia
• \Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system\Rare isolated myopia
• \Disease\Disorder of body system\Visual system disorder\Disorder of vision\Disorder of refraction AND/OR accommodation\Disorder of refraction\Myopia\Severe myopia\Rare isolated myopia

Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3726300011	Rare isolated myopia	en	Synonym	Active	Case insensitive	SNOMED CT core
3726301010	Rare isolated myopia (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3726302015	A rare genetic refraction anomaly disorder with characteristics of non-syndromic severe myopia, which may be associated with cataract and vitreoretinal degeneration (retinal detachment) that may lead to blindness.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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