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111385000: Tay-Sachs disease (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
178623012 Tay-Sachs disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
187763014 Severe hexosaminidase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
187764015 TSD en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
187765019 Amaurotic familial idiocy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
187766018 Infantile amaurotic familial disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
189395019 GM>2< gangliosidosis, type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
361785018 Hexosaminidase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
630949018 Tay-Sachs disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
894341000172116 déficit en hexosaminidase A fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
915701000172114 maladie de Tay-Sachs fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Tay-Sachs disease Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Tay-Sachs disease Is a GM2 gangliosidosis (disorder) true Inferred relationship Some
Tay-Sachs disease Finding site Structure of nervous system (body structure) true Inferred relationship Some 2
Tay-Sachs disease Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
B variant hexosaminidase A deficiency Is a True Tay-Sachs disease Inferred relationship Some
B1 variant hexosaminidase A deficiency Is a True Tay-Sachs disease Inferred relationship Some
Tay-Sachs disease, variant AB Is a True Tay-Sachs disease Inferred relationship Some
Family history of Tay-Sachs disease Associated finding True Tay-Sachs disease Inferred relationship Some 1

This concept is not in any reference sets

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