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1187543005: Dystrophy of retina due to GM2 gangliosidosis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4674116014 Retinal dystrophy due to GM2 gangliosidosis en Synonym Active Only initial character case insensitive SNOMED CT core module
4674524010 Dystrophy of retina due to GM2 gangliosidosis en Synonym Active Only initial character case insensitive SNOMED CT core module
4674525011 Dystrophy of retina due to GM2 gangliosidosis (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dystrophy of retina due to GM2 gangliosidosis Is a Retinal dystrophy true Inferred relationship Existential restriction modifier
Dystrophy of retina due to GM2 gangliosidosis Due to GM2 gangliosidosis true Inferred relationship Existential restriction modifier 2
Dystrophy of retina due to GM2 gangliosidosis Finding site Retinal structure true Inferred relationship Existential restriction modifier 1
Dystrophy of retina due to GM2 gangliosidosis Associated morphology Dystrophy 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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