441188004: Homozygous protein C deficiency (disorder)

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

\Functional finding\Disorder of hemostatic system\...

\Thrombophilia\Hereditary thrombophilia (disorder)\Hereditary protein C deficiency (disorder)\Homozygous protein C deficiency
\Thrombophilia\Protein C deficiency disease\Hereditary protein C deficiency (disorder)\Homozygous protein C deficiency

\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Deficiency of naturally occurring coagulation factor inhibitor\Protein C deficiency disease\Hereditary protein C deficiency (disorder)\Homozygous protein C deficiency

\Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia (disorder)\Hereditary protein C deficiency (disorder)\Homozygous protein C deficiency
\Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Hereditary protein C deficiency (disorder)\Homozygous protein C deficiency
\Disease\Disorder of hemostatic system\Thrombophilia\Protein C deficiency disease\Hereditary protein C deficiency (disorder)\Homozygous protein C deficiency
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Deficiency of naturally occurring coagulation factor inhibitor\Protein C deficiency disease\Hereditary protein C deficiency (disorder)\Homozygous protein C deficiency

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

2788436010 Homozygous protein C deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2794654010 Homozygous protein C deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2788436010 Homozygous protein C deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2794654010 Homozygous protein C deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5333441000241112 déficit en protéine C, homozygote fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5333441000241112 déficit en protéine C, homozygote fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Homozygous protein C deficiency	Is a	Hereditary protein C deficiency (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Homozygous protein C deficiency	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Homozygous protein C deficiency	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder)	Is a	True	Homozygous protein C deficiency	Inferred relationship	Existential restriction modifier (core metadata concept)
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder)	Due to	True	Homozygous protein C deficiency	Inferred relationship	Existential restriction modifier (core metadata concept)	6

This concept is not in any reference sets