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

\Blood coagulation disorder\Deficiency of naturally occurring coagulation factor inhibitor\Protein C deficiency disease\Hereditary protein C deficiency (disorder)\Homozygous protein C deficiency (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia (disorder)\Hereditary protein C deficiency (disorder)\Homozygous protein C deficiency (disorder)
\Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Hereditary protein C deficiency (disorder)\Homozygous protein C deficiency (disorder)
\Disease\Disorder of hemostatic system\Thrombophilia\Protein C deficiency disease\Hereditary protein C deficiency (disorder)\Homozygous protein C deficiency (disorder)
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Deficiency of naturally occurring coagulation factor inhibitor\Protein C deficiency disease\Hereditary protein C deficiency (disorder)\Homozygous protein C 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

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

5734491000172114 déficit en protéine C, homozygote fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

4909561000172112 homozygote proteïne C-deficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

4909571000172115 homozygote deficiëntie van proteïne C nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Homozygous protein C deficiency (disorder)	Is a	Hereditary protein C deficiency (disorder)	true	Inferred relationship	Some
Homozygous protein C deficiency (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Homozygous protein C deficiency (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	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 (disorder)	Inferred relationship	Some
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder)	Due to	True	Homozygous protein C deficiency (disorder)	Inferred relationship	Some	6

This concept is not in any reference sets