439145006: Congenital hypofibrinogenemia (disorder)

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

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

\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Congenital hypofibrinogenemia (disorder)

\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital hypofibrinogenemia (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital hypofibrinogenemia (disorder)
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Congenital hypofibrinogenemia (disorder)
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital hypofibrinogenemia (disorder)
\Disease\Congenital disease (disorder)\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Congenital hypofibrinogenemia (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

2789363016 Congenital hypofibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2794588013 Congenital hypofibrinogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2794589017 Congenital hypofibrinogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2503741000052114 kongenital hypofibrinogenemi sv Synonym (core metadata concept) Active Entire term 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
Congenital hypofibrinogenemia (disorder)	Is a	Hereditary factor I deficiency disease	true	Inferred relationship	Some
Congenital hypofibrinogenemia (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Congenital hypofibrinogenemia (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	2
Congenital hypofibrinogenemia (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	2

Inbound Relationships

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Group

This concept is not in any reference sets