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719455002: Cone dystrophy with supernormal rod response (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3316424013 Cone dystrophy with supernormal rod response (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3316425014 Cone dystrophy with supernormal rod response en Synonym Active Entire term case insensitive SNOMED CT core module
3316426010 Cone dystrophy with supernormal rod electroretinogram en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cone dystrophy with supernormal rod response Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Cone dystrophy with supernormal rod response Is a Cone dystrophy true Inferred relationship Existential restriction modifier
Cone dystrophy with supernormal rod response Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Cone dystrophy with supernormal rod response Finding site Retinal structure false Inferred relationship Existential restriction modifier 1
Cone dystrophy with supernormal rod response Finding site Cone of retina true Inferred relationship Existential restriction modifier 1
Cone dystrophy with supernormal rod response Finding site Rod of retina true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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