50189006: Hereditary factor XIII deficiency disease (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 coagulation factor deficiency\Hereditary factor XIII deficiency disease

\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor XIII deficiency disease\Hereditary factor XIII deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease

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

Descriptions:

Id Description Lang Type Status Case? Module

83596013 Hereditary factor XIII deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
83597016 Laki-Lorand factor deficiency disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
787949018 Hereditary factor XIII deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2032291000052114 ärftlig faktor XIII-brist sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary factor XIII deficiency disease	Is a	Factor XIII deficiency disease	true	Inferred relationship	Some
Hereditary factor XIII deficiency disease	Interprets	Nutritional deficiency (finding)	false	Inferred relationship	Some
Hereditary factor XIII deficiency disease	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Hereditary factor XIII deficiency disease	Finding site	Body system structure	false	Inferred relationship	Some
Hereditary factor XIII deficiency disease	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Hereditary factor XIII deficiency disease	Is a	Hereditary coagulation factor deficiency	true	Inferred relationship	Some
Hereditary factor XIII deficiency disease	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hereditary factor XIII deficiency disease	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary factor XIII A subunit and B subunit deficiency (disorder)	Is a	True	Hereditary factor XIII deficiency disease	Inferred relationship	Some
Hereditary factor XIII B subunit deficiency (disorder)	Is a	True	Hereditary factor XIII deficiency disease	Inferred relationship	Some
Hereditary factor XIII A subunit deficiency (disorder)	Is a	True	Hereditary factor XIII deficiency disease	Inferred relationship	Some

This concept is not in any reference sets