128113003: ziekte van von Willebrand type 2A subtype IB (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Functional finding\Disorder of hemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 1\Hereditary von Willebrand disease type 1B

\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 1\Hereditary von Willebrand disease type 1B
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary von Willebrand disease type 1\Hereditary von Willebrand disease type 1B
\Disease\Disorder of hemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 1\Hereditary von Willebrand disease type 1B

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

194707019 von Willebrand disease type IB en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

206399013 Hereditary von Willebrand disease type IB en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3891029013 Hereditary von Willebrand disease type 1B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5156378010 Hereditary von Willebrand disease type 1B (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

9484831000146112 ziekte van von Willebrand type 2A subtype IB nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

9484841000146116 ziekte van von Willebrand type 2A subtype IB (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary von Willebrand disease type 1B	Is a	ziekte van von Willebrand type 2A	false	Inferred relationship	Some
Hereditary von Willebrand disease type 1B	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Hereditary von Willebrand disease type 1B	Occurrence	Congenital	false	Inferred relationship	Some	2
Hereditary von Willebrand disease type 1B	Finding site	Body system structure	false	Inferred relationship	Some
Hereditary von Willebrand disease type 1B	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Hereditary von Willebrand disease type 1B	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hereditary von Willebrand disease type 1B	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Hereditary von Willebrand disease type 1B	Is a	Hereditary von Willebrand disease type 1	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets