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128107007: Hereditary von Willebrand disease type 2 (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
194701018 von Willebrand disease type 2 en Synonym Active Entire term case sensitive SNOMED CT core module
206397010 Hereditary von Willebrand disease type 2 en Synonym Active Only initial character case insensitive SNOMED CT core module
732068011 von Willebrand disease type 2 (disorder) en Fully specified name Inactive Entire term case sensitive SNOMED CT core module
5156380016 Hereditary von Willebrand disease type 2 (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary von Willebrand disease type 2 Is a von Willebrand disorder false Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 2 Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 2 Finding site Body system structure false Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 2 Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 2 Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Hereditary von Willebrand disease type 2 Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1
Hereditary von Willebrand disease type 2 Is a Autosomal hereditary disorder false Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 2 Is a Hereditary von Willebrand disease true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary von Willebrand disease type 2N Is a True Hereditary von Willebrand disease type 2 Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 2A Is a True Hereditary von Willebrand disease type 2 Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 2B Is a True Hereditary von Willebrand disease type 2 Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 2M Is a True Hereditary von Willebrand disease type 2 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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