439157002: Hereditary combined coagulation factor deficiency (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Functional finding\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Includes both quantitative and qualitative disorders of procoagulants\...

\Combined coagulation factor deficiency\Hereditary combined coagulation factor deficiency (disorder)

\Hereditary coagulation factor deficiency\Hereditary combined coagulation factor deficiency (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary combined coagulation factor deficiency (disorder)
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Includes both quantitative and qualitative disorders of procoagulants\Combined coagulation factor deficiency\Hereditary combined coagulation factor deficiency (disorder)
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Includes both quantitative and qualitative disorders of procoagulants\Hereditary coagulation factor deficiency\Hereditary combined coagulation factor deficiency (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2787558013 Hereditary combined coagulation factor deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2795244014 Hereditary combined coagulation factor deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

6275061000241111 déficit héréditaire de plusieurs facteurs de coagulation fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6275071000241115 déficit héréditaire combiné en facteurs de coagulation fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary combined coagulation factor deficiency (disorder)	Is a	Combined coagulation factor deficiency	true	Inferred relationship	Some
Hereditary combined coagulation factor deficiency (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hereditary combined coagulation factor deficiency (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Hereditary combined coagulation factor deficiency (disorder)	Is a	Hereditary coagulation factor deficiency	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
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	True	Hereditary combined coagulation factor deficiency (disorder)	Inferred relationship	Some
Combined vitamin K-dependent clotting factors deficiency (VKCFD) is a congenital bleeding disorder resulting from variably decreased levels of coagulation factors II, VII, IX and X, as well as natural anticoagulants protein C, protein S and protein Z.	Is a	True	Hereditary combined coagulation factor deficiency (disorder)	Inferred relationship	Some

This concept is not in any reference sets