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764969006: Biallelic RPE65, retinoid isomerohydrolase mutation associated retinal dystrophy (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3655849015 Biallelic RPE65, retinoid isomerohydrolase mutation associated retinal dystrophy (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3655850015 Biallelic RPE65 mutation associated retinal dystrophy en Synonym Active Initial character case insensitive SNOMED CT core
3655851016 Biallelic RPE65, retinoid isomerohydrolase mutation associated retinal dystrophy en Synonym Active Initial character case insensitive SNOMED CT core
3655854012 Biallelic mutation carriers have a mutation (not necessarily the same mutation) in both copies of a particular gene (a paternal and a maternal mutation). The RPE65 gene provides instructions for making an enzyme that is essential for normal vision and mutations in this gene result in reduced or absent levels of RPE65 activity, blocking the visual cycle and resulting in impaired vision. Almost all patients eventually progress to complete blindness. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Biallelic RPE65 mutation associated retinal dystrophy Is a Congenital disease true Inferred relationship Some
Biallelic RPE65 mutation associated retinal dystrophy Is a Hereditary retinal dystrophy primarily involving retinal pigment epithelium true Inferred relationship Some
Biallelic RPE65 mutation associated retinal dystrophy Associated morphology Dystrophy true Inferred relationship Some 1
Biallelic RPE65 mutation associated retinal dystrophy Occurrence Congenital true Inferred relationship Some 1
Biallelic RPE65 mutation associated retinal dystrophy Finding site Retinal structure true Inferred relationship Some 1

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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