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128107007: von Willebrand disease type 2 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
194701018 von Willebrand disease type 2 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
206397010 Hereditary von Willebrand disease type 2 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
518001000241118 maladie de von Willebrand type 2 (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
732068011 von Willebrand disease type 2 (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
972201000172117 maladie de von Willebrand type 2 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
von Willebrand disease type 2 interprète (attribut) Hemostatic function (observable entity) true Inferred relationship Some 1
von Willebrand disease type 2 a pour interprétation (attribut) anormal true Inferred relationship Some 1
von Willebrand disease type 2 est un(e) (attribut) Autosomal hereditary disorder true Inferred relationship Some
von Willebrand disease type 2 est un(e) (attribut) maladie de von Willebrand true Inferred relationship Some
von Willebrand disease type 2 localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
von Willebrand disease type 2 est défini par la manifestation de (attribut) constatation sur le système hémostatique false Inferred relationship Some
von Willebrand disease type 2 localisation d'une constatation (attribut) Entire hematological system (body structure) false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
von Willebrand disease type 2N est un(e) (attribut) True von Willebrand disease type 2 Inferred relationship Some
Hereditary von Willebrand disease type 2A est un(e) (attribut) True von Willebrand disease type 2 Inferred relationship Some
Hereditary von Willebrand disease type 2B est un(e) (attribut) True von Willebrand disease type 2 Inferred relationship Some
Hereditary von Willebrand disease type 2M est un(e) (attribut) True von Willebrand disease type 2 Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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