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128114009: Hereditary von Willebrand disease type 1C (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
194708012 von Willebrand disease type IC en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
206400018 Hereditary von Willebrand disease type IC en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3891027010 Hereditary von Willebrand disease type 1C en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5156379019 Hereditary von Willebrand disease type 1C (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 1C Is a von Willebrand disease type 2M false Inferred relationship Some
Hereditary von Willebrand disease type 1C Finding site Entire hematological system (body structure) false Inferred relationship Some
Hereditary von Willebrand disease type 1C Finding site Body system structure false Inferred relationship Some
Hereditary von Willebrand disease type 1C Has definitional manifestation Hemostatic system finding false Inferred relationship Some
Hereditary von Willebrand disease type 1C Interprets Hemostatic function true Inferred relationship Some 1
Hereditary von Willebrand disease type 1C Has interpretation Abnormal true Inferred relationship Some 1
Hereditary von Willebrand disease type 1C 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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