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111589005: Dysfibrinogenemia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
178844010 Dysfibrinogenemia en Synonym Active Case insensitive SNOMED CT core
363901010 Dysfibrinogenaemia en Synonym Active Case insensitive SNOMED CT core
632834017 Dysfibrinogenemia (disorder) en Fully specified name Active Case insensitive SNOMED CT core


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dysfibrinogenaemia Interprets Haemostatic function true Inferred relationship Some 1
Dysfibrinogenaemia Has interpretation Abnormal true Inferred relationship Some 1
Dysfibrinogenaemia Occurrence Congenital true Inferred relationship Some 2
Dysfibrinogenaemia Finding site Body system structure false Inferred relationship Some
Dysfibrinogenaemia Has definitional manifestation Haemostatic system finding false Inferred relationship Some
Dysfibrinogenaemia Is a Factor I deficiency disease true Inferred relationship Some
Dysfibrinogenaemia Finding site Entire haematological system false Inferred relationship Some
Dysfibrinogenaemia Is a Congenital fibrinogen abnormality true Inferred relationship Some
Dysfibrinogenaemia Is a Coagulation factor deficiency syndrome false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary dysfibrinogenaemia Is a True Dysfibrinogenaemia Inferred relationship Some
Alpha chain defect dysfibrinogenaemia Is a True Dysfibrinogenaemia Inferred relationship Some
Beta chain defect dysfibrinogenaemia Is a True Dysfibrinogenaemia Inferred relationship Some
Gamma chain defect dysfibrinogenaemia Is a True Dysfibrinogenaemia Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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