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128115005: Pseudo von Willebrand 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
194709016 Pseudo von Willebrand disease en Synonym Active Only initial character case insensitive SNOMED CT core module
732077016 Pseudo von Willebrand disease (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
5156402014 Platelet type-von Willebrand disease en Synonym Active Only initial character case insensitive SNOMED CT core module
5156403016 Pseudo-von Willebrand disease type 2B en Synonym Active Only initial character case insensitive SNOMED CT core module
5156404010 PT-VWD - platelet type-von Willebrand disease en Synonym Active Entire term case sensitive SNOMED CT core module
5156406012 Platelet type pseudo-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
Pseudo von Willebrand disease Is a Blood coagulation disorder true Inferred relationship Existential restriction modifier
Pseudo von Willebrand disease Is a Hereditary disorder of hematologic system false Inferred relationship Existential restriction modifier
Pseudo von Willebrand disease Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Pseudo von Willebrand disease Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Pseudo von Willebrand disease Is a Hereditary disorder by system false Inferred relationship Existential restriction modifier
Pseudo von Willebrand disease Finding site Body system structure false Inferred relationship Existential restriction modifier
Pseudo von Willebrand disease Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Pseudo von Willebrand disease Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Pseudo von Willebrand disease Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1
Pseudo von Willebrand disease Is a Hereditary platelet function disorder true Inferred relationship Existential restriction modifier
Pseudo von Willebrand disease Finding site Body system structure true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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