773771008: zeldzame geïsoleerde myopie (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Eye / vision finding\Visual system disorder\...

\Hereditary disorder of the visual system (disorder)\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 (disorder)\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 (disorder)\Rare isolated myopia
\Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system (disorder)\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, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3726300011 Rare isolated myopia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3726301010 Rare isolated myopia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

6590191000146112 zeldzame geïsoleerde myopie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6590201000146114 zeldzame geïsoleerde myopie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

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 Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Rare isolated myopia	Is a	Hereditary disorder of the visual system (disorder)	true	Inferred relationship	Some
Rare isolated myopia	Is a	Severe myopia	true	Inferred relationship	Some
Rare isolated myopia	Is a	Autosomal hereditary disorder	true	Inferred relationship	Some
Rare isolated myopia	Finding site	Structure of visual system (body structure)	true	Inferred relationship	Some	1

Inbound Relationships

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This concept is not in any reference sets