439459008: Hereditary factor XIII 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 B subunit deficiency

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

\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease\Hereditary factor XIII 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 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 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:

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
2789395015	Hereditary factor XIII B subunit deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2790347018	Hereditary factor XIII B subunit deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2790348011	Hereditary factor XIII beta subunit deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2790527013	Hereditary factor XIII type III deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2789395015	Hereditary factor XIII B subunit deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2790347018	Hereditary factor XIII B subunit deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2790348011	Hereditary factor XIII beta subunit deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2790527013	Hereditary factor XIII type III deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6314881000241114	déficit héréditaire en sous-unité B facteur Laki-Lorand	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6314891000241111	déficit héréditaire en facteur XIIIb de la coagulation	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6314901000241112	déficit héréditaire en sous-unité B du facteur de stabilisation de la fibrine	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6314881000241114	déficit héréditaire en sous-unité B facteur Laki-Lorand	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6314891000241111	déficit héréditaire en facteur XIIIb de la coagulation	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6314901000241112	déficit héréditaire en sous-unité B du facteur de stabilisation de la fibrine	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module