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439725008: déficit en disintégrine et en métalloprotéinase avec thrombospondine de type I, motif 13 (ADAMTS13) (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2790002014 A disintegrin and metalloproteinase with thrombospondin type 1 motif 13 deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2792405011 A disintegrin and metalloproteinase with thrombospondin type 1 motif 13 deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2795389012 A disintegrin and metalloproteinase with thrombospondin type 1 motif 13 deficiency (ADAMTS13) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
352411000077119 déficit en disintégrine et en métalloprotéinase avec thrombospondine de type I, motif 13 (ADAMTS13) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
637941000077115 déficit en disintégrine et en métalloprotéinase avec thrombospondine de type I, motif 13 (ADAMTS13) (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A disintegrin and metalloproteinase with thrombospondin type 1 motif 13 deficiency (disorder) interprète (attribut) Hemostatic function (observable entity) true Inferred relationship Some 1
A disintegrin and metalloproteinase with thrombospondin type 1 motif 13 deficiency (disorder) a pour interprétation (attribut) anormal true Inferred relationship Some 1
A disintegrin and metalloproteinase with thrombospondin type 1 motif 13 deficiency (disorder) est un(e) (attribut) Disorder of haemostatic system true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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