111589005: Dysfibrinogenemia (disorder)

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

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

\Fibrinogen abnormality\Congenital fibrinogen abnormality\Dysfibrinogenemia

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

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

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

178844010 Dysfibrinogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
189812014 Dysfibrinogenemia, NOS en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
363901010 Dysfibrinogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
632834017 Dysfibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5592361000172113 dysfibrinogénémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
9004621000172113 anomalie de la coagulation causée par la production d'un fibrinogène anormal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4067841000172111 dysfibrinogenemie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Dysfibrinogenemia	Is a	Congenital fibrinogen abnormality	true	Inferred relationship	Some
Dysfibrinogenemia	Is a	Coagulation factor deficiency syndrome	false	Inferred relationship	Some
Dysfibrinogenemia	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Dysfibrinogenemia	Occurrence	Congenital	true	Inferred relationship	Some	2
Dysfibrinogenemia	Finding site	Body system structure	false	Inferred relationship	Some
Dysfibrinogenemia	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Dysfibrinogenemia	Is a	Factor I deficiency disease (disorder)	true	Inferred relationship	Some
Dysfibrinogenemia	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Dysfibrinogenemia	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Alpha chain defect dysfibrinogenemia	Is a	True	Dysfibrinogenemia	Inferred relationship	Some
Beta chain defect dysfibrinogenaemia	Is a	True	Dysfibrinogenemia	Inferred relationship	Some
Gamma chain defect dysfibrinogenaemia	Is a	True	Dysfibrinogenemia	Inferred relationship	Some
Hereditary dysfibrinogenemia (disorder)	Is a	True	Dysfibrinogenemia	Inferred relationship	Some

Reference Sets

Belgian subset for medical problems in patient health records