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717407006: Congenital plasminogen activator inhibitor deficiency type 1 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3309285015 Congenital plasminogen activator inhibitor deficiency type 1 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3309286019 Congenital plasminogen activator inhibitor deficiency type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401575017 A rare hemorrhagic disorder due to a constitutional hemostatic factors defect characterized by premature lysis of hemostatic clots and a moderate bleeding tendency. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401576016 A rare haemorrhagic disorder due to a constitutional haemostatic factors defect characterised by premature lysis of haemostatic clots and a moderate bleeding tendency. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital plasminogen activator inhibitor deficiency type 1 (disorder) Is a Hereditary coagulation factor deficiency true Inferred relationship Some
Congenital plasminogen activator inhibitor deficiency type 1 (disorder) Is a Congenital disease (disorder) true Inferred relationship Some
Congenital plasminogen activator inhibitor deficiency type 1 (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Congenital plasminogen activator inhibitor deficiency type 1 (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital plasminogen activator inhibitor deficiency type 1 (disorder) Has interpretation Abnormal true Inferred relationship Some 2
Congenital plasminogen activator inhibitor deficiency type 1 (disorder) Interprets Hemostatic function true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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