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50189006: Hereditary factor XIII deficiency disease (disorder)

\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

787949018 Hereditary factor XIII deficiency disease (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

83596013 Hereditary factor XIII deficiency disease en Synonym Active Initial character case insensitive SNOMED CT core

83597016 Laki-Lorand factor deficiency disease en Synonym Active Case sensitive SNOMED CT core

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary factor XIII deficiency disease	Interprets	Haemostatic function	true	Inferred relationship	Some	1
Hereditary factor XIII deficiency disease	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Hereditary factor XIII deficiency disease	Is a	Factor XIII deficiency disease	true	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	Haemostatic 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	Nutritional deficiency	false	Inferred relationship	Some
Hereditary factor XIII deficiency disease	Finding site	Entire haematological system	false	Inferred relationship	Some

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

Reference Sets

Australian emergency department reference set

Id	Description	Lang	Type	Status	Case?	Module
787949018	Hereditary factor XIII deficiency disease (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
83596013	Hereditary factor XIII deficiency disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
83597016	Laki-Lorand factor deficiency disease	en	Synonym	Active	Case sensitive	SNOMED CT core