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234473003: Platelet type von Willebrand's disease (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
351306019 Platelet type von Willebrand's disease en Synonym Active Only initial character case insensitive SNOMED CT core module
622798017 Platelet type von Willebrand's disease (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
2839594017 Platelet type von Willebrand disease en Synonym Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

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

This concept is not in any reference sets

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