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40855001: Hereditary factor VII deficiency disease (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Functional finding\Disorder of hemostatic system\Blood coagulation disorder\...

\Prothrombin complex deficiency\Factor VII deficiency\Hereditary factor VII deficiency disease (disorder)

\Coagulation factor deficiency syndrome\Factor VII deficiency\Hereditary factor VII deficiency disease (disorder)
\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor VII deficiency disease (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor VII deficiency disease (disorder)
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Prothrombin complex deficiency\Factor VII deficiency\Hereditary factor VII deficiency disease (disorder)
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor VII deficiency\Hereditary factor VII deficiency disease (disorder)
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor VII deficiency disease (disorder)

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

Descriptions:

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Belgian GP subset (foundation metadata concept)

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
68137016	Hereditary factor VII deficiency syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
68138014	Hereditary hypoproconvertinemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
492809012	Hereditary hypoproconvertinaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2789802015	Hereditary factor VII deficiency disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2794698010	Hereditary factor VII deficiency disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1891921000172111	déficience congénitale en facteur de coagulation VII	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
8961181000172111	déficit congénital en facteur VII	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
9004011000172110	hypoproconvertinémie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
9004021000172117	déficit constitutionnel en proconvertine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
1891931000172114	congenitale hereditaire stollingsfactor VII deficiëntie	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)