234465007: Alpha-2-antiplasmin deficiency (disorder)

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

\Functional finding\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Disorder involving the fibrinolytic system\Fibrinolytic bleeding syndrome\Alpha-2-antiplasmin deficiency

\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Disorder involving the fibrinolytic system\Fibrinolytic bleeding syndrome\Alpha-2-antiplasmin deficiency

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

351298013 Alpha-2-antiplasmin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

622788011 Alpha-2-antiplasmin deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4995721000241117 déficit en alpha-2-antiplasmine 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
Alpha-2-antiplasmin deficiency	Is a	Fibrinolytic bleeding syndrome	true	Inferred relationship	Some
Alpha-2-antiplasmin deficiency	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Alpha-2-antiplasmin deficiency	Finding site	Body system structure	false	Inferred relationship	Some
Alpha-2-antiplasmin deficiency	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Alpha-2-antiplasmin deficiency	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Alpha-2-antiplasmin deficiency	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
A rare hemorrhagic disorder caused by congenital deficiency of alpha2 antiplasmin, leading to dysregulated fibrinolysis and is characterized by a hemorrhagic tendency presenting from childhood with prolonged bleeding and ecchymoses following minor trauma and spontaneous bleeding episodes (often in unusual locations like diaphysis of long bones).	Is a	True	Alpha-2-antiplasmin deficiency	Inferred relationship	Some

This concept is not in any reference sets