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:

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

2032361000052112 ärftlig faktor VII-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 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
Bleeding in hereditary factor VII deficiency disease (finding)	Associated with	True	Hereditary factor VII deficiency disease (disorder)	Inferred relationship	Some	1

This concept is not in any reference sets