234446004: Congenital von Willebrand's disease (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

351268018 Congenital von Willebrand's disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

351269014 vWD - Congenital von Willebrand's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

622765010 Congenital von Willebrand's disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2839593011 Congenital von Willebrand disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

110611000077117 maladie de von Willebrand congénitale fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Congenital von Willebrand's disease type I	Is a	False	maladie de von Willebrand congénitale	Inferred relationship	Some
Congenital von Willebrand's disease type II	Is a	False	maladie de von Willebrand congénitale	Inferred relationship	Some
Congenital von Willebrand's disease type III	Is a	False	maladie de von Willebrand congénitale	Inferred relationship	Some
von Willebrand disease, type IIF	Is a	False	maladie de von Willebrand congénitale	Inferred relationship	Some
Hereditary von Willebrand disease type 1A	Is a	False	maladie de von Willebrand congénitale	Inferred relationship	Some
von Willebrand disease, type 1^a^	Is a	False	maladie de von Willebrand congénitale	Inferred relationship	Some
von Willebrand disease type IA	Is a	False	maladie de von Willebrand congénitale	Inferred relationship	Some
maladie de von Willebrand type 2A	Is a	False	maladie de von Willebrand congénitale	Inferred relationship	Some
maladie de von Willebrand type 2B	Is a	False	maladie de von Willebrand congénitale	Inferred relationship	Some

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set (foundation metadata concept)