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33316007: GM2 gangliosidosis (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1009151000172119 gangliosidose à GM2 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
2989571016 GM 2 gangliosidosis (disorder) en Fully specified name Inactive Entire term case sensitive (core metadata concept) SNOMED CT core
2989659015 GM 2 gangliosidosis en Synonym (core metadata concept) Inactive Entire term case sensitive (core metadata concept) SNOMED CT core
418481000241113 gangliosidose à GM2 (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
4553711018 GM2 gangliosidosis (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
485484018 GM2 gangliosidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
55589016 GM>2< gangliosidosis en Synonym (core metadata concept) Inactive Entire term case sensitive (core metadata concept) SNOMED CT core
55590013 GM>2< gangliosidosis, NOS en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
55591012 Deficiency of beta-N-acetylhexosaminidase isoenzymes en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
764704012 GM>2< gangliosidosis (disorder) en Fully specified name Inactive Entire term case sensitive (core metadata concept) SNOMED CT core

14 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
gangliosidose à GM2 est un(e) (attribut) gangliosidose (trouble) true Inferred relationship Some
gangliosidose à GM2 survenue (attribut) congénital true Inferred relationship Some 1
gangliosidose à GM2 localisation d'une constatation (attribut) système nerveux true Inferred relationship Some 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Retinal dystrophy due to GM2 gangliosidosis Due to True gangliosidose à GM2 Inferred relationship Some 2
Sandhoff disease est un(e) (attribut) True gangliosidose à GM2 Inferred relationship Some
Adult chronic GM2 gangliosidosis (disorder) est un(e) (attribut) True gangliosidose à GM2 Inferred relationship Some
Infantile GM2 gangliosidosis (disorder) est un(e) (attribut) True gangliosidose à GM2 Inferred relationship Some
Juvenile GM2 gangliosidosis (disorder) est un(e) (attribut) True gangliosidose à GM2 Inferred relationship Some
Tay-Sachs disease est un(e) (attribut) True gangliosidose à GM2 Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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