234447008: Congenital von Willebrand's disease type I (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

351270010 vWD - Congenital von Willebrand's disease type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

351271014 Congenital von Willebrand's disease type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

622766011 Congenital von Willebrand's disease type I (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2841830016 Congenital von Willebrand disease type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5954561000172113 maladie de von Willebrand type I, congénitale fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

4608401000172116 congenitale ziekte van von Willebrand type 1 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
maladie de von Willebrand type I, congénitale	Is a	maladie congénitale de von Willebrand	false	Inferred relationship	Some
maladie de von Willebrand type I, congénitale	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
maladie de von Willebrand type I, congénitale	Occurrence	Congenital	false	Inferred relationship	Some	1
maladie de von Willebrand type I, congénitale	Finding site	Body system structure	false	Inferred relationship	Some
maladie de von Willebrand type I, congénitale	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
maladie de von Willebrand type I, congénitale	Has interpretation	Abnormal	false	Inferred relationship	Some	2
maladie de von Willebrand type I, congénitale	Interprets	Hemostatic function	false	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set (foundation metadata concept)