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


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

Descriptions:

Id Description Lang Type Status Case? Module
4674116014 Retinal dystrophy due to GM2 gangliosidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4674524010 Dystrophy of retina due to GM2 gangliosidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4674525011 Dystrophy of retina due to GM2 gangliosidosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5327941000052113 retinal dystrofi orsakad av GM>2< gangliosidos sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinal dystrophy due to GM2 gangliosidosis Is a Retinal dystrophy true Inferred relationship Some
Retinal dystrophy due to GM2 gangliosidosis Due to GM2 gangliosidosis (disorder) true Inferred relationship Some 2
Retinal dystrophy due to GM2 gangliosidosis Finding site Retinal structure true Inferred relationship Some 1
Retinal dystrophy due to GM2 gangliosidosis Associated morphology Dystrophy true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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