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716746003: Congenital alpha-2-antiplasmin deficiency (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3307409016 Congenital alpha-2-antiplasmin deficiency (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3307410014 Congenital alpha-2-antiplasmin deficiency en Synonym Active Case insensitive SNOMED CT core
3307411013 Congenital alpha2-antiplasmin deficiency en Synonym Active Case insensitive SNOMED CT core
3307412018 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. Inherited in an autosomal recessive manner. en Definition Active Case sensitive SNOMED CT core
3307413011 A rare haemorrhagic disorder caused by congenital deficiency of alpha2 antiplasmin, leading to dysregulated fibrinolysis and is characterised by a haemorrhagic tendency presenting from childhood with prolonged bleeding and ecchymoses following minor trauma and spontaneous bleeding episodes. Inherited in an autosomal recessive manner. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital alpha-2-antiplasmin deficiency Has interpretation Abnormal true Inferred relationship Some 2
Congenital alpha-2-antiplasmin deficiency Interprets Haemostatic function true Inferred relationship Some 2
Congenital alpha-2-antiplasmin deficiency Is a Congenital disease true Inferred relationship Some
Congenital alpha-2-antiplasmin deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Congenital alpha-2-antiplasmin deficiency Is a Alpha-2-antiplasmin deficiency true Inferred relationship Some
Congenital alpha-2-antiplasmin deficiency Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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