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26029002: Mild 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
2787929017 Mild hereditary factor VIII deficiency disease (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
2792392016 Mild hereditary factor VIII deficiency disease en Synonym Active Initial character case insensitive SNOMED CT core
43600019 Mild hemophilia A en Synonym Active Initial character case insensitive SNOMED CT core
483093012 Mild haemophilia A en Synonym Active Initial character case insensitive SNOMED CT core
2884517012 Mild disease manifests factor VIII activity of greater than 5% of normal en Definition Active Case sensitive SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Mild hereditary factor VIII deficiency disease with inhibitor Is a True Mild hereditary factor VIII deficiency disease Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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