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128096008: Hereditary platelet function disorder (disorder)

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
194690019 Hereditary platelet function disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
732056019 Hereditary platelet function disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
194690019 Hereditary platelet function disorder en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
194690019 Hereditary platelet function disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
732056019 Hereditary platelet function disorder (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
732056019 Hereditary platelet function disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4787601000241118 anomalie héréditaire de la fonction plaquettaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4787601000241118 anomalie héréditaire de la fonction plaquettaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

28 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary platelet function disorder (disorder) Is a Inherited platelet disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary platelet function disorder (disorder) Is a Hereditary disorder of haematologic sysem false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary platelet function disorder (disorder) Is a Qualitative platelet disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary platelet function disorder (disorder) Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary platelet function disorder (disorder) Finding site Platelet (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary platelet function disorder (disorder) Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary platelet function disorder (disorder) Has definitional manifestation Platelet finding false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary platelet function disorder (disorder) Has definitional manifestation Hemostatic system finding (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary platelet function disorder (disorder) Is a Qualitative platelet disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary platelet function disorder (disorder) Finding site Body system structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary platelet function disorder (disorder) Interprets Hemostatic function true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary platelet function disorder (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Platelet type pseudo-von Willebrand disease Is a False Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Scott syndrome Is a True Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Platelet storage pool defect Is a True Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Familial alpha>2< adrenergic receptor defect in platelets Is a True Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Isolated collagen aggregation defect Is a True Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Glanzmann's thrombasthenia Is a True Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Platelet procoagulant activity deficiency Is a True Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Platelet secretory disorder (disorder) Is a True Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Bernard Soulier syndrome Is a True Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I (disorder) Is a True Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
P2Y12 defect is a rare hemorrhagic disorder characterized by mild to moderate bleeding diathesis with easy bruising, mucosal bleeding, and excessive post-operative hemorrhage due to defect of the platelet P2Y12 receptor resulting in selective impairment of platelet responses to adenosine diphosphate. Is a True Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Bleeding diathesis due to collagen receptor defect (disorder) Is a True Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) Is a True Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Severe autosomal recessive macrothrombocytopenia (disorder) Is a True Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Pseudo von Willebrand disease Is a True Hereditary platelet function disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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