439460003: hereditaire deficiëntie van subunit A en subunit B van stollingsfactor XIII (aandoening)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Functional finding\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\...
• \Factor XIII deficiency disease\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency (disorder)
• \Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency (disorder)
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor XIII deficiency disease\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency (disorder)
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency (disorder)

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
6489611000146113	hereditaire deficiëntie van subunit A en subunit B van factor XIII	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6489631000146118	erfelijke FXIII-deficiëntie type I	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9891361000146116	hereditaire deficiëntie van subunit A en subunit B van stollingsfactor XIII (aandoening)	nl	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9892851000146119	hereditaire deficiëntie van subunit A en subunit B van stollingsfactor XIII	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Reference Sets

Description inactivation indicator reference set

GB English

US English

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