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715559004: Combined deficiency of factor V and factor VIII (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5400960010 A rare inherited bleeding disorder due to the reduction in activity and antigen levels of both factor V (FV) and factor VIII (FVIII) and characterized by mild-to-moderate bleeding symptoms. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400961014 A rare inherited bleeding disorder due to the reduction in activity and antigen levels of both factor V (FV) and factor VIII (FVIII) and characterised by mild-to-moderate bleeding symptoms. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3303019018 Combined deficiency of factor V and factor VIII (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303020012 Combined deficiency of factor V and factor VIII en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303021011 Factor V and factor VIII combined deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303022016 Familial multiple coagulation factor deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
927451000172116 déficit combiné en FV et FVIII fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1017591000172110 déficit combiné en facteurs V et VIII fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3384721001000115 Kombinierter Mangel an Faktor V und Faktor VIII de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare inherited bleeding disorder due to the reduction in activity and antigen levels of both factor V (FV) and factor VIII (FVIII) and characterized by mild-to-moderate bleeding symptoms. Is a Factor V deficiency true Inferred relationship Some
A rare inherited bleeding disorder due to the reduction in activity and antigen levels of both factor V (FV) and factor VIII (FVIII) and characterized by mild-to-moderate bleeding symptoms. Is a Autosomal recessive hereditary disorder true Inferred relationship Some
A rare inherited bleeding disorder due to the reduction in activity and antigen levels of both factor V (FV) and factor VIII (FVIII) and characterized by mild-to-moderate bleeding symptoms. Is a Factor VIII deficiency true Inferred relationship Some
A rare inherited bleeding disorder due to the reduction in activity and antigen levels of both factor V (FV) and factor VIII (FVIII) and characterized by mild-to-moderate bleeding symptoms. Is a Hereditary combined coagulation factor deficiency (disorder) true Inferred relationship Some
A rare inherited bleeding disorder due to the reduction in activity and antigen levels of both factor V (FV) and factor VIII (FVIII) and characterized by mild-to-moderate bleeding symptoms. Interprets Hemostatic function true Inferred relationship Some 1
A rare inherited bleeding disorder due to the reduction in activity and antigen levels of both factor V (FV) and factor VIII (FVIII) and characterized by mild-to-moderate bleeding symptoms. Has interpretation Abnormal true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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