234472008: defect van glycoproteïne Ib (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\Platelet membrane defect\Glycoprotein Ib defect

\Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ib defect

\Functional finding\Disorder of hemostatic system\Platelet disorder\Inherited platelet disorder\Platelet membrane defect\Glycoprotein Ib defect

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

351305015 Glycoprotein Ib defect en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
622796018 Glycoprotein Ib defect (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
6476301000146118 defect van glycoproteïne Ib nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6476311000146116 GP Ib-defect nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6476321000146114 defect van glycoproteïne Ib (aandoening) nl Fully specified name Active Only initial character 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
Glycoprotein Ib defect	Is a	Platelet membrane defect	true	Inferred relationship	Some
Glycoprotein Ib defect	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Glycoprotein Ib defect	Finding site	Platelet	false	Inferred relationship	Some
Glycoprotein Ib defect	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Glycoprotein Ib defect	Has definitional manifestation	Platelet finding	false	Inferred relationship	Some
Glycoprotein Ib defect	Finding site	Body system structure	false	Inferred relationship	Some
Glycoprotein Ib defect	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Glycoprotein Ib defect	Finding site	Body system structure	false	Inferred relationship	Some	1
Glycoprotein Ib defect	Has interpretation	Abnormal	true	Inferred relationship	Some	2
Glycoprotein Ib defect	Interprets	Hemostatic function	true	Inferred relationship	Some	2
Glycoprotein Ib defect	Finding site	Body system structure	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Platelet type von Willebrand's disease	Is a	False	Glycoprotein Ib defect	Inferred relationship	Some
Bernard Soulier syndrome	Is a	True	Glycoprotein Ib defect	Inferred relationship	Some

This concept is not in any reference sets