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717941005: Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5401642017 A rare genetic skin disease characterized by severe skin laxity affecting the trunk and limbs. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401643010 A rare genetic skin disease characterised by severe skin laxity affecting the trunk and limbs. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3324406013 Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3324407016 Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3324408014 PXE (pseudoxanthoma elasticum) like syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3324409018 Pseudoxanthoma elasticum-like syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
870251000172112 syndrome PXE (pseudoxanthome élastique)-like fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
928711000172112 hyperlaxité de la peau par déficit en facteur de coagulation dépendant de la vitamine K fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3410651001000119 Hyperlaxität der Haut durch Mangel an Vitamin K-abhängigen Koagulationsfaktoren de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare genetic skin disease characterized by severe skin laxity affecting the trunk and limbs. Due to Includes both quantitative and qualitative disorders of procoagulants true Inferred relationship Some 2
A rare genetic skin disease characterized by severe skin laxity affecting the trunk and limbs. Is a Collagen and elastic tissue disorders affecting skin true Inferred relationship Some
A rare genetic skin disease characterized by severe skin laxity affecting the trunk and limbs. Finding site Skin structure true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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