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16872008: Severe hereditary factor VIII deficiency disease (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2788401011 Severe hereditary factor VIII deficiency disease (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
2795425017 Severe hereditary factor VIII deficiency disease en Synonym Active Initial character case insensitive SNOMED CT core
28565012 Severe hemophilia A en Synonym Active Initial character case insensitive SNOMED CT core
477973011 Severe haemophilia A en Synonym Active Initial character case insensitive SNOMED CT core
2884791011 Severe disease manifests factor VIII activity of less than 1%, except in the U.K. and Italy, where severe disease includes factor VIII activity levels of less than 2% en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Severe hereditary factor VIII deficiency disease Interprets Haemostatic function true Inferred relationship Some 1
Severe hereditary factor VIII deficiency disease Has interpretation Abnormal true Inferred relationship Some 1
Severe hereditary factor VIII deficiency disease Is a Hereditary factor VIII deficiency disease true Inferred relationship Some
Severe hereditary factor VIII deficiency disease Severity Severe false Inferred relationship Some
Severe hereditary factor VIII deficiency disease Finding site Body system structure false Inferred relationship Some
Severe hereditary factor VIII deficiency disease Has definitional manifestation Haemostatic system finding false Inferred relationship Some
Severe hereditary factor VIII deficiency disease 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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