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312917007: Cone dystrophy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
456725016 Cone dystrophy en Synonym Active Entire term case insensitive SNOMED CT core module
709642015 Cone dystrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cone dystrophy Is a Hereditary retinal dystrophy true Inferred relationship Existential restriction modifier
Cone dystrophy Finding site Retinal structure false Inferred relationship Existential restriction modifier
Cone dystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Cone dystrophy Finding site Retinal structure false Inferred relationship Existential restriction modifier 1
Cone dystrophy Finding site Cone of retina true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Progressive cone dystrophy (without rod involvement) Is a True Cone dystrophy Inferred relationship Existential restriction modifier
Cone dystrophy with supernormal rod response Is a True Cone dystrophy Inferred relationship Existential restriction modifier
Retinohepatoendocrinologic syndrome Is a True Cone dystrophy Inferred relationship Existential restriction modifier
Achromatopsia Is a True Cone dystrophy Inferred relationship Existential restriction modifier
Blue cone monochromatism Is a True Cone dystrophy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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