154818001: Congenital afibrinogenemia (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 afibrinogenaemia

\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital afibrinogenaemia

\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital afibrinogenaemia
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Congenital afibrinogenaemia
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease\Congenital afibrinogenaemia
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Congenital afibrinogenaemia

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

240815017 Congenital afibrinogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
240816016 Congenital afibrinogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
535079011 Congenital afibrinogenaemia en Fully specified name Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
2753725011 Congenital afibrinogenaemia (disorder) en Fully specified name Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
2788877018 Congenital afibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital afibrinogenaemia	Is a	Hereditary factor I deficiency disease	true	Inferred relationship	Some
Congenital afibrinogenaemia	Occurrence	Congenital	true	Inferred relationship	Some	1
Congenital afibrinogenaemia	Has interpretation	Abnormal	true	Inferred relationship	Some	2
Congenital afibrinogenaemia	Interprets	Hemostatic function	true	Inferred relationship	Some	2

Inbound Relationships

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This concept is not in any reference sets