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80328002: Progressive cone-rod dystrophy (disorder)


Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1234464015 Cone-rod retinal dystrophy en Synonym Active Case insensitive SNOMED CT core
133294010 Progressive cone-rod dystrophy en Synonym Active Case insensitive SNOMED CT core
821476014 Progressive cone-rod dystrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4594938019 A rare retinal dystrophy with characteristics of photophobia, progressive loss of visual acuity, nystagmus, visual field abnormalities, abnormal color vision, and psychophysical and electrophysiological evidence of abnormal cone function. Progressive cone dystrophy usually presents in childhood or early adult life, and patients tend to develop rod photoreceptor dysfunction in later life. en Definition Active Case sensitive SNOMED CT core
4594939010 A rare retinal dystrophy with characteristics of photophobia, progressive loss of visual acuity, nystagmus, visual field abnormalities, abnormal colour vision, and psychophysical and electrophysiological evidence of abnormal cone function. Progressive cone dystrophy usually presents in childhood or early adult life, and patients tend to develop rod photoreceptor dysfunction in later life. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Progressive cone-rod dystrophy Is a Hereditary degenerative disease of central nervous system true Inferred relationship Some
Progressive cone-rod dystrophy Is a Chronic nervous system disorder true Inferred relationship Some
Progressive cone-rod dystrophy Is a Disorder of visual pathways true Inferred relationship Some
Progressive cone-rod dystrophy Clinical course Progressive true Inferred relationship Some 2
Progressive cone-rod dystrophy Finding site Neuroepithelial layer true Inferred relationship Some 1
Progressive cone-rod dystrophy Is a Autosomal hereditary disorder true Inferred relationship Some
Progressive cone-rod dystrophy Is a Hereditary retinal dystrophy true Inferred relationship Some
Progressive cone-rod dystrophy Associated morphology Dystrophy true Inferred relationship Some 1
Progressive cone-rod dystrophy Finding site Retinal structure false Inferred relationship Some 1
Progressive cone-rod dystrophy Finding site Retinal structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Is a False Progressive cone-rod dystrophy Inferred relationship Some

Reference Sets

Emergency department reference set

Australian emergency department reference set

NSW Emergency Department reference set

Clinical finding foundation reference set

Emergency department diagnosis reference set

Problem/Diagnosis reference set

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