441101007: Heterozygous 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)\Heterozygous protein C deficiency (disorder)
\Thrombophilia\Protein C deficiency disease\Hereditary protein C deficiency (disorder)\Heterozygous protein C deficiency (disorder)

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

\Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia (disorder)\Hereditary protein C deficiency (disorder)\Heterozygous protein C deficiency (disorder)
\Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Hereditary protein C deficiency (disorder)\Heterozygous protein C deficiency (disorder)
\Disease\Disorder of hemostatic system\Thrombophilia\Protein C deficiency disease\Hereditary protein C deficiency (disorder)\Heterozygous 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)\Heterozygous 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

2790011014 Heterozygous protein C deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2791270019 Heterozygous protein C deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5757601000172111 déficit en protéine C, hétérozygote fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

4943311000172114 heterozygote proteïne C-deficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

4943321000172116 heterozygote 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
Heterozygous protein C deficiency (disorder)	Is a	Hereditary protein C deficiency (disorder)	true	Inferred relationship	Some
Heterozygous protein C deficiency (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Heterozygous protein C deficiency (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Belgian subset for medical problems in patient health records