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716663009: Severe early childhood onset retinal dystrophy (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3307131017 Severe early childhood onset retinal dystrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3307132012 Severe early childhood onset retinal dystrophy en Synonym Active Case insensitive SNOMED CT core
3307135014 SECORD - Severe early childhood onset retinal dystrophy en Synonym Active Case sensitive SNOMED CT core
3307136010 An inherited retinal dystrophy with manifestation of severe congenital night blindness, progressive retinal dystrophy and nystagmus. Blindness is often complete by the age of 30 years. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Severe early childhood onset retinal dystrophy Is a Hereditary retinal dystrophy true Inferred relationship Some
Severe early childhood onset retinal dystrophy Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Severe early childhood onset retinal dystrophy Associated morphology Dystrophy true Inferred relationship Some 1
Severe early childhood onset retinal dystrophy Occurrence Early childhood true Inferred relationship Some 1
Severe early childhood onset 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

Unit of use quantity reference set

Description inactivation indicator reference set

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