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52311001: Homocystinemia (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
87046017 Homocystinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
496277018 Homocystinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
790307019 Homocystinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1810031000195113 omocistinemia it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
557881000172118 homocystinémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
590391000172115 homocystinemia fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Homocystinemia Is a Disorder of sulphur-bearing amino acid metabolism true Inferred relationship Some
Homocystinemia Occurrence Congenital false Inferred relationship Some
Homocystinemia Finding site Body system structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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