359725000: hereditaire ziekte van von Willebrand type 2M (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 2\Hereditary von Willebrand disease type 2M

\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 2\Hereditary von Willebrand disease type 2M
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary von Willebrand disease type 2M
\Disease\Disorder of hemostatic system\Blood coagulation disorder\von Willebrand disorder\Hereditary von Willebrand disease\Hereditary von Willebrand disease type 2\Hereditary von Willebrand disease type 2M

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

474870017 Hereditary von Willebrand disease type 2M en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

734045018 Hereditary von Willebrand disease type 2M (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

6657951000146118 hereditaire ziekte van von Willebrand type 2M (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6657961000146115 hereditaire ziekte van von Willebrand type 2M nl Synonym (core metadata concept) 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 2M	Is a	von Willebrand disorder	false	Inferred relationship	Some
Hereditary von Willebrand disease type 2M	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Hereditary von Willebrand disease type 2M	Finding site	Body system structure	false	Inferred relationship	Some
Hereditary von Willebrand disease type 2M	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Hereditary von Willebrand disease type 2M	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hereditary von Willebrand disease type 2M	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Hereditary von Willebrand disease type 2M	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Hereditary von Willebrand disease type 2M	Is a	Hereditary von Willebrand disease type 2	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets