FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

359732009: Hereditary von Willebrand disease type 2N (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
474895016 von Willebrand disease type 2N en Synonym Active Entire term case sensitive SNOMED CT core module
5156384013 Hereditary von Willebrand disease type 2N (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
5156385014 Hereditary von Willebrand disease type 2N 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
Hereditary von Willebrand disease type 2N Is a von Willebrand disorder false Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 2N Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 2N Finding site Body system structure false Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 2N Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 2N Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Hereditary von Willebrand disease type 2N Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1
Hereditary von Willebrand disease type 2N Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 2N Is a Hereditary von Willebrand disease type 2 true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
von Willebrand Normandy screening test Has focus True Hereditary von Willebrand disease type 2N Inferred relationship Existential restriction modifier 2

This concept is not in any reference sets

Back to Start