439460003: Hereditary factor XIII A subunit and B subunit deficiency (disorder)

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

\Functional finding\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\...

\Factor XIII deficiency disease\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency

\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency

\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\Factor XIII deficiency disease\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency

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

2789756019 Hereditary factor XIII A subunit and B subunit deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2790528015 Hereditary factor XIII type I deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2794133016 Hereditary factor XIII A subunit and B subunit deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2789756019 Hereditary factor XIII A subunit and B subunit deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2790528015 Hereditary factor XIII type I deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2794133016 Hereditary factor XIII A subunit and B subunit deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary factor XIII A subunit and B subunit deficiency	Is a	Hereditary factor XIII deficiency disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary factor XIII A subunit and B subunit deficiency	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary factor XIII A subunit and B subunit deficiency	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

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Reference Sets

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