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359732009: Hereditary von Willebrand disease type 2N (disorder)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
474895016 von Willebrand disease type 2N en Synonym Active Case sensitive SNOMED CT core
5156384013 Hereditary von Willebrand disease type 2N (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
5156385014 Hereditary von Willebrand disease type 2N en Synonym Active Initial character case insensitive SNOMED CT core
734275018 von Willebrand disease type 2N (disorder) en Fully specified name Inactive Case sensitive SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
von Willebrand disease type 2N Interprets Haemostatic function true Inferred relationship Some 1
von Willebrand disease type 2N Has interpretation Abnormal true Inferred relationship Some 1
von Willebrand disease type 2N Is a Autosomal recessive hereditary disorder true Inferred relationship Some
von Willebrand disease type 2N Is a von Willebrand disease type 2 true Inferred relationship Some
von Willebrand disease type 2N Is a von Willebrand disorder false Inferred relationship Some
von Willebrand disease type 2N Finding site Body system structure false Inferred relationship Some
von Willebrand disease type 2N Has definitional manifestation Haemostatic system finding false Inferred relationship Some
von Willebrand disease type 2N Finding site Entire haematological system false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
von Willebrand Normandy screening test Has focus True von Willebrand disease type 2N Inferred relationship Some 2

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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