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359700009: Hereditary von Willebrand disease type 1A (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
474740015 Hereditary von Willebrand disease type IA en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3891028017 Hereditary von Willebrand disease type 1A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5156374012 Hereditary von Willebrand disease type 1A (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


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

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