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234472008: Glycoprotein Ib defect (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
351305015 Glycoprotein Ib defect en Synonym Active Only initial character case insensitive SNOMED CT core module
622796018 Glycoprotein Ib defect (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Glycoprotein Ib defect Is a Platelet membrane defect true Inferred relationship Existential restriction modifier
Glycoprotein Ib defect Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Glycoprotein Ib defect Finding site Platelet false Inferred relationship Existential restriction modifier
Glycoprotein Ib defect Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Glycoprotein Ib defect Has definitional manifestation Platelet finding false Inferred relationship Existential restriction modifier
Glycoprotein Ib defect Finding site Body system structure false Inferred relationship Existential restriction modifier
Glycoprotein Ib defect Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Glycoprotein Ib defect Finding site Body system structure false Inferred relationship Existential restriction modifier 1
Glycoprotein Ib defect Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Glycoprotein Ib defect Interprets Hemostatic function true Inferred relationship Existential restriction modifier 2
Glycoprotein Ib defect Finding site Body system structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Platelet type von Willebrand's disease Is a True Glycoprotein Ib defect Inferred relationship Existential restriction modifier
Bernard Soulier syndrome Is a True Glycoprotein Ib defect Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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