234456000: Congenital fibrinogen abnormality (disorder)

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

\Functional finding\Disorder of hemostatic system\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality

\Disease\Disorder of hemostatic system\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality
\Disease\Congenital disease (disorder)\Congenital fibrinogen abnormality

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

351284017 Congenital fibrinogen abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
622778010 Congenital fibrinogen abnormality (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
110621000077110 anomalie congénitale du fibrinogène fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hypofibrinogenaemia	Is a	False	Congenital fibrinogen abnormality	Inferred relationship	Some
Hypodysfibrinogenaemia	Is a	True	Congenital fibrinogen abnormality	Inferred relationship	Some
Dysfibrinogenemia	Is a	True	Congenital fibrinogen abnormality	Inferred relationship	Some
Hereditary factor I deficiency disease	Is a	True	Congenital fibrinogen abnormality	Inferred relationship	Some

This concept is not in any reference sets