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232062002: Hereditary vitreoretinopathy (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
347713018 Hereditary vitreoretinopathy en Synonym Active Case insensitive SNOMED CT core
620078011 Hereditary vitreoretinopathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary vitreoretinopathy Is a Inherited disorder of connective tissue true Inferred relationship Some
Hereditary vitreoretinopathy Is a Retinopathy false Inferred relationship Some
Hereditary vitreoretinopathy Finding site Retinal structure true Inferred relationship Some 2
Hereditary vitreoretinopathy Is a Disorder of vitreous body true Inferred relationship Some
Hereditary vitreoretinopathy Finding site Vitreous body structure true Inferred relationship Some 1
Hereditary vitreoretinopathy Is a Retinal disorder true Inferred relationship Some
Hereditary vitreoretinopathy Is a Hereditary disorder of the visual system true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Stickler syndrome Is a True Hereditary vitreoretinopathy Inferred relationship Some
Familial exudative vitreoretinopathy Is a True Hereditary vitreoretinopathy Inferred relationship Some
Wagner syndrome Is a True Hereditary vitreoretinopathy Inferred relationship Some
Goldmann-Favre syndrome Is a False Hereditary vitreoretinopathy Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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