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770434009: Familial benign flecked retina (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3700846017 Familial benign flecked retina en Synonym Active Case insensitive SNOMED CT core
3700847014 Familial benign flecked retina (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3700848016 A rare retinal dystrophy with characteristics of diffuse bilateral white-yellow fleck-like lesions extending to the far periphery of the retina but sparing the foveal region, with asymptomatic clinical phenotype and absence of electrophysiologic deficits. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial benign flecked retina Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Familial benign flecked retina Finding site Retinal structure true Inferred relationship Some 1
Familial benign flecked retina Is a Hereditary retinal dystrophy true Inferred relationship Some
Familial benign flecked retina Is a Retinal flecking true Inferred relationship Some
Familial benign flecked retina Finding site Retinal structure true Inferred relationship Some 2
Familial benign flecked retina Associated morphology Dystrophy true Inferred relationship Some 1
Familial benign flecked retina Associated morphology Deposition true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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