234475005: defect in generatie van tromboxaan (aandoening)

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

\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood (disorder)\...

\Hereditary disorder of cellular element of blood (disorder)\Inherited platelet disorder\Thromboxane generation defect

\Platelet disorder\Inherited platelet disorder\Thromboxane generation defect

\Functional finding\Disorder of hemostatic system\Platelet disorder\Inherited platelet disorder\Thromboxane generation defect

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Inherited platelet disorder\Thromboxane generation defect
\Disease\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Inherited platelet disorder\Thromboxane generation defect
\Disease\Disorder of cellular component of blood (disorder)\Platelet disorder\Inherited platelet disorder\Thromboxane generation defect
\Disease\Disorder of hemostatic system\Platelet disorder\Inherited platelet disorder\Thromboxane generation defect
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Inherited platelet disorder\Thromboxane generation defect

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

351309014 Thromboxane generation defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

622800012 Thromboxane generation defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

6544601000146114 defect in Tx-generatie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6544611000146111 defect in generatie van tromboxaan (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6544621000146118 defect in generatie van tromboxaan nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Thromboxane generation defect	Is a	Inherited platelet disorder	true	Inferred relationship	Some
Thromboxane generation defect	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Thromboxane generation defect	Finding site	Platelet	false	Inferred relationship	Some
Thromboxane generation defect	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Thromboxane generation defect	Has definitional manifestation	Platelet finding	false	Inferred relationship	Some
Thromboxane generation defect	Finding site	Body system structure	false	Inferred relationship	Some
Thromboxane generation defect	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Thromboxane generation defect	Finding site	Body system structure	true	Inferred relationship	Some	2
Thromboxane generation defect	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Thromboxane generation defect	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Cyclooxygenase deficiency	Is a	True	Thromboxane generation defect	Inferred relationship	Some
Thromboxane synthetase deficiency	Is a	True	Thromboxane generation defect	Inferred relationship	Some

This concept is not in any reference sets