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128106003: Hereditary von Willebrand disease type 1 (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
194700017 von Willebrand disease type 1 en Synonym Active Entire term case sensitive SNOMED CT core module
206396018 Hereditary von Willebrand disease type 1 en Synonym Active Only initial character case insensitive SNOMED CT core module
732067018 von Willebrand disease type 1 (disorder) en Fully specified name Inactive Entire term case sensitive SNOMED CT core module
5156373018 Hereditary von Willebrand disease type 1 (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

3 descendants. Search Descendants:

Expanded Value Set

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

This concept is not in any reference sets

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