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716663009: Severe early childhood onset retinal dystrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3307131017 Severe early childhood onset retinal dystrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3307132012 Severe early childhood onset retinal dystrophy en Synonym Active Entire term case insensitive SNOMED CT core module
3307135014 SECORD - Severe early childhood onset retinal dystrophy en Synonym Active Entire term case sensitive SNOMED CT core module


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 Existential restriction modifier
Severe early childhood onset retinal dystrophy Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Severe early childhood onset retinal dystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Severe early childhood onset retinal dystrophy Occurrence Early childhood true Inferred relationship Existential restriction modifier 1
Severe early childhood onset retinal dystrophy Finding site Retinal structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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