FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

128105004: von Willebrand disorder (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
5156398017 Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
194699018 von Willebrand disorder en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
474294014 Vascular haemophilia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474295010 Angiohemophilia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474296011 Pseudohemophilia type B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
474297019 Vascular hemophilia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474298012 Pseudohaemophilia type B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
474299016 Constitutional thrombopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474301011 Factor VIII deficiency with vascular defect en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
474302016 von Willebrand disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
474303014 vWD - von Willebrand's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
474304015 von Willebrand disease, platelet type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
474305019 von Willebrand's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
474306018 von Willebrand-Jurgens disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
474307010 Angiohaemophilia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
732066010 von Willebrand disorder (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1815401000195117 disturbo di von Willebrand it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
159061000172117 maladie de von Willebrand fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
384301000274111 Willebrand-Jürgens-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
670731000274112 Angiohämophilie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3450681001000119 Von-Willebrand-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

13 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Is a Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system. true Inferred relationship Some
Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Finding site Entire hematological system (body structure) false Inferred relationship Some
Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Finding site Body system structure false Inferred relationship Some
Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Has definitional manifestation Hemostatic system finding false Inferred relationship Some
Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Interprets Hemostatic function true Inferred relationship Some 1
Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Has interpretation Abnormal true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
maladie de von Willebrand congénitale Is a False Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some
A rare bleeding disorder characterized by defects in von Willebrand factor, similar to those seen in hereditary von Willebrand disease (VWD), but which are caused by an underlying pathology, generally in elderly patients without any personal or family history of bleeding anomalies. Is a True Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some
A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a partial, quantitative plasmatic deficiency of an otherwise structurally and functionally normal von Willebrand factor (VWF). Is a False Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some
A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (VWF). Depending on the type of functional abnormalities, this form is classified as type 2A, 2B, 2M or 2N. Is a False Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some
A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a total or near-total absence of Willebrand factor (VWF) in the plasma and cellular compartments, also leading to a profound deficiency of plasmatic factor VIII (FVIII). It is the most severe form of VWD. Is a False Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some
Hereditary von Willebrand disease type 2A Is a False Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some
Hereditary von Willebrand disease type 2B Is a False Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some
Hereditary von Willebrand disease type 2M Is a False Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some
maladie de von Willebrand type 2M Is a False Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some
Hereditary von Willebrand disease type 2N (disorder) Is a False Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some
von Willebrand disease Normandy Is a False Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some
Acquired von Willebrand syndrome Is a False Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some
von Willebrand screening test (procedure) Has focus True Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some 2
Family history of Von Willebrand disease (situation) Associated finding True Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some 1
von Willebrand factor below reference range Is a False Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some
A rare, inherited bleeding disorder characterized by defective platelet adhesion and secondary coagulation defect that manifests as abnormal bleeding of variable severity occurring either spontaneously or in association with an invasive procedure. Three main subtypes are defined based on the type of von Willebrand factor defect: partial (type 1) or total (type 3) deficiency, and qualitative/functional anomalies (type 2). Is a True Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome. Inferred relationship Some

This concept is not in any reference sets

Back to Start