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1187252002: autosomaal dominante trombocytopenie met secretiedefect van trombocyt (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4672939015 Autosomal dominant thrombocytopenia with platelet secretion defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4672940018 Autosomal dominant thrombocytopenia with platelet secretion defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
13240501000146115 autosomaal dominante trombocytopenie met secretiedefect van trombocyt nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13240511000146118 autosomaal dominante trombocytopenie met secretiedefect van trombocyt (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13304781000146112 autosomaal dominante trombopenie met gestoorde secretie van bloedplaatje nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
4672941019 A rare isolated constitutional thrombocytopenia characterized by reduced platelet count and defective platelet ATP secretion, resulting in increased bleeding tendency. Clinical manifestations are easy bruising, gum bleeding, menorrhagia, spontaneous epistaxis, spontaneous muscle hematoma and potential postpartum hemorrhage among others. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4672942014 A rare isolated constitutional thrombocytopenia characterised by reduced platelet count and defective platelet ATP secretion, resulting in increased bleeding tendency. Clinical manifestations are easy bruising, gum bleeding, menorrhagia, spontaneous epistaxis, spontaneous muscle haematoma and potential postpartum haemorrhage among others. 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
Autosomal dominant thrombocytopenia with platelet secretion defect Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant thrombocytopenia with platelet secretion defect Is a Hereditary thrombocytopenic disorder (disorder) true Inferred relationship Some
Autosomal dominant thrombocytopenia with platelet secretion defect Is a Platelet secretory disorder true Inferred relationship Some
Autosomal dominant thrombocytopenia with platelet secretion defect Interprets Hemostatic function true Inferred relationship Some 2
Autosomal dominant thrombocytopenia with platelet secretion defect Has interpretation Abnormal true Inferred relationship Some 2
Autosomal dominant thrombocytopenia with platelet secretion defect Interprets Platelet count true Inferred relationship Some 3
Autosomal dominant thrombocytopenia with platelet secretion defect Has interpretation Below reference range true Inferred relationship Some 3
Autosomal dominant thrombocytopenia with platelet secretion defect Finding site Body system structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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