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128114009: Hereditary von Willebrand disease type 1C (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
194708012 von Willebrand disease type IC en Synonym Active Case sensitive SNOMED CT core
206400018 Hereditary von Willebrand disease type IC en Synonym Active Initial character case insensitive SNOMED CT core
3891027010 Hereditary von Willebrand disease type 1C en Synonym Active Initial character case insensitive SNOMED CT core
5156379019 Hereditary von Willebrand disease type 1C (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
von Willebrand disease type IC Interprets Haemostatic function true Inferred relationship Some 1
von Willebrand disease type IC Has interpretation Abnormal true Inferred relationship Some 1
von Willebrand disease type IC Is a von Willebrand disease type 1 true Inferred relationship Some
von Willebrand disease type IC Is a von Willebrand disease type 2M false Inferred relationship Some
von Willebrand disease type IC Finding site Body system structure false Inferred relationship Some
von Willebrand disease type IC Has definitional manifestation Haemostatic system finding false Inferred relationship Some
von Willebrand disease type IC Finding site Entire haematological system false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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