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359725000: Hereditary von Willebrand disease type 2M (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
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
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
3454181001000118 Von-Willebrand-Syndrom Typ 2M de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5223681000241114 maladie de von Willebrand type 2M, héréditaire fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5223681000241114 maladie de von Willebrand type 2M, héréditaire fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3454181001000118 Von-Willebrand-Syndrom Typ 2M de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary von Willebrand disease type 2M (disorder) Is a von Willebrand disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary von Willebrand disease type 2M (disorder) Finding site Entire hematological system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary von Willebrand disease type 2M (disorder) Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary von Willebrand disease type 2M (disorder) Has definitional manifestation Hemostatic system finding (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary von Willebrand disease type 2M (disorder) Interprets Hemostatic function true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary von Willebrand disease type 2M (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary von Willebrand disease type 2M (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary von Willebrand disease type 2M (disorder) Is a Hereditary von Willebrand disease type 2 true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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