439145006: congenitale hypofibrinogenemie (aandoening)

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 foetus and/or newborn\Congenital disease (disorder)\Congenital fibrinogen abnormality\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)

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

6448281000146119 congenitale hypofibrinogenemie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6448291000146117 congenitale hypofibrinogenemie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6448301000146118 aangeboren hypofibrinogenemie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands 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

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets