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783194008: Bleeding diathesis due to thromboxane synthesis deficiency (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3758027013 Bleeding diathesis due to thromboxane synthesis deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3758028015 Bleeding diathesis due to thromboxane synthesis deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3758029011 A rare genetic isolated constitutional thrombocytopenia disease with characteristics of impaired platelet aggregation resulting from a defect in thromboxane synthesis or signaling, manifesting with mild to moderate mucocutaneous, gastrointestinal or surgical bleeding (for example easy bruising, prolonged epistaxis, excessive bleeding after a tooth extraction). Conferred by heterozygous mutation in the gene encoding the thromboxane A2 receptor (TBXA2R) on chromosome 19p13. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3758027013 Bleeding diathesis due to thromboxane synthesis deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3758028015 Bleeding diathesis due to thromboxane synthesis deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3758029011 A rare genetic isolated constitutional thrombocytopenia disease with characteristics of impaired platelet aggregation resulting from a defect in thromboxane synthesis or signaling, manifesting with mild to moderate mucocutaneous, gastrointestinal or surgical bleeding (for example easy bruising, prolonged epistaxis, excessive bleeding after a tooth extraction). Conferred by heterozygous mutation in the gene encoding the thromboxane A2 receptor (TBXA2R) on chromosome 19p13. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3442211001000110 Hämorrhagische Diathese durch Thromboxan-Synthetase-Mangel de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5787991000241113 diathèse hémorragique due à un déficit de synthèse de la thromboxane fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5787991000241113 diathèse hémorragique due à un déficit de synthèse de la thromboxane fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3442211001000110 Hämorrhagische Diathese durch Thromboxan-Synthetase-Mangel de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Bleeding diathesis due to thromboxane synthesis deficiency (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Bleeding diathesis due to thromboxane synthesis deficiency (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Bleeding diathesis due to thromboxane synthesis deficiency (disorder) Is a Congenital thrombocytopaenia true Inferred relationship Existential restriction modifier (core metadata concept)
Bleeding diathesis due to thromboxane synthesis deficiency (disorder) Interprets Platelet count true Inferred relationship Existential restriction modifier (core metadata concept) 1
Bleeding diathesis due to thromboxane synthesis deficiency (disorder) Is a Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system. false Inferred relationship Existential restriction modifier (core metadata concept)
Bleeding diathesis due to thromboxane synthesis deficiency (disorder) Interprets Hemostatic function true Inferred relationship Existential restriction modifier (core metadata concept) 4
Bleeding diathesis due to thromboxane synthesis deficiency (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 4
Bleeding diathesis due to thromboxane synthesis deficiency (disorder) Due to Thromboxane synthetase deficiency true Inferred relationship Existential restriction modifier (core metadata concept) 3
Bleeding diathesis due to thromboxane synthesis deficiency (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Bleeding diathesis due to thromboxane synthesis deficiency (disorder) Is a thrombocytopénie secondaire true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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