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234470000: Platelet membrane defect (disorder)

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

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

\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Platelet membrane defect (disorder)

\Platelet disorder\Inherited platelet disorder\Platelet membrane defect (disorder)

\Functional finding\Disorder of hemostatic system\Platelet disorder\Inherited platelet disorder\Platelet membrane defect (disorder)

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

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Platelet membrane defect (disorder)	Is a	Inherited platelet disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Platelet membrane defect (disorder)	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Platelet membrane defect (disorder)	Finding site	Platelet (cell structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Platelet membrane defect (disorder)	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Platelet membrane defect (disorder)	Has definitional manifestation	Platelet finding	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Platelet membrane defect (disorder)	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Platelet membrane defect (disorder)	Has definitional manifestation	Hemostatic system finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Platelet membrane defect (disorder)	Finding site	Body system structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Platelet membrane defect (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Platelet membrane defect (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Glycoprotein Ia defect	Is a	True	Platelet membrane defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Glycoprotein Ib defect	Is a	True	Platelet membrane defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Glanzmann's thrombasthenia	Is a	True	Platelet membrane defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Bleeding disorder due to glycoprotein VI deficiency (disorder)	Is a	True	Platelet membrane defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
351303010	Platelet membrane defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
622794015	Platelet membrane defect (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
351303010	Platelet membrane defect	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
351303010	Platelet membrane defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
622794015	Platelet membrane defect (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
622794015	Platelet membrane defect (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4995741000241113	défaut de membrane plaquettaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4995741000241113	défaut de membrane plaquettaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module