45366001: hereditaire dysfibrinogenemie (aandoening)

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

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

\Fibrinogen abnormality\Congenital fibrinogen abnormality\...

\Dysfibrinogenemia\Hereditary dysfibrinogenemia (disorder)

\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia (disorder)

\Coagulation factor deficiency syndrome\Factor I deficiency disease (disorder)\Dysfibrinogenemia\Hereditary dysfibrinogenemia (disorder)
\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia (disorder)

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

75627010 Congenital dysfibrinogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

494185015 Congenital dysfibrinogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2786838014 Hereditary dysfibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2792832010 Hereditary dysfibrinogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2795322018 Hereditary dysfibrinogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1462881000146113 hereditaire dysfibrinogenemie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

1462891000146110 hereditaire dysfibrinogenemie 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
Hereditary dysfibrinogenemia (disorder)	Is a	Dysfibrinogenemia	true	Inferred relationship	Some
Hereditary dysfibrinogenemia (disorder)	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Hereditary dysfibrinogenemia (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Hereditary dysfibrinogenemia (disorder)	Finding site	Body system structure	false	Inferred relationship	Some
Hereditary dysfibrinogenemia (disorder)	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Hereditary dysfibrinogenemia (disorder)	Is a	Hereditary factor I deficiency disease	true	Inferred relationship	Some
Hereditary dysfibrinogenemia (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	2
Hereditary dysfibrinogenemia (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary thrombophilic dysfibrinogenemia (disorder)	Is a	True	Hereditary dysfibrinogenemia (disorder)	Inferred relationship	Some

This concept is not in any reference sets