439459008: Hereditary factor XIII B subunit deficiency (disorder)

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 B subunit deficiency (disorder)

\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease\Hereditary factor XIII B subunit deficiency (disorder)

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

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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary factor XIII B subunit deficiency (disorder)	Is a	Hereditary factor XIII deficiency disease	true	Inferred relationship	Some
Hereditary factor XIII B subunit deficiency (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hereditary factor XIII B subunit deficiency (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships

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This concept is not in any reference sets