FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

128096008: Hereditary platelet function disorder (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
194690019 Hereditary platelet function disorder en Synonym Active Entire term case insensitive SNOMED CT core module
732056019 Hereditary platelet function disorder (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


28 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary platelet function disorder Is a Inherited platelet disorder true Inferred relationship Existential restriction modifier
Hereditary platelet function disorder Is a Hereditary disorder of hematologic system false Inferred relationship Existential restriction modifier
Hereditary platelet function disorder Is a Qualitative platelet disorder false Inferred relationship Existential restriction modifier
Hereditary platelet function disorder Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Hereditary platelet function disorder Finding site Platelet false Inferred relationship Existential restriction modifier
Hereditary platelet function disorder Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Hereditary platelet function disorder Has definitional manifestation Platelet finding false Inferred relationship Existential restriction modifier
Hereditary platelet function disorder Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Hereditary platelet function disorder Is a Qualitative platelet disorder true Inferred relationship Existential restriction modifier
Hereditary platelet function disorder Finding site Body system structure true Inferred relationship Existential restriction modifier 2
Hereditary platelet function disorder Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Hereditary platelet function disorder Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Platelet type pseudo-von Willebrand disease Is a False Hereditary platelet function disorder Inferred relationship Existential restriction modifier
Scott syndrome Is a True Hereditary platelet function disorder Inferred relationship Existential restriction modifier
Platelet storage pool defect Is a True Hereditary platelet function disorder Inferred relationship Existential restriction modifier
Familial alpha>2< adrenergic receptor defect in platelets Is a True Hereditary platelet function disorder Inferred relationship Existential restriction modifier
Isolated collagen aggregation defect Is a True Hereditary platelet function disorder Inferred relationship Existential restriction modifier
Glanzmann's thrombasthenia Is a True Hereditary platelet function disorder Inferred relationship Existential restriction modifier
Platelet procoagulant activity deficiency Is a True Hereditary platelet function disorder Inferred relationship Existential restriction modifier
Platelet secretory disorder Is a True Hereditary platelet function disorder Inferred relationship Existential restriction modifier
Bernard Soulier syndrome Is a True Hereditary platelet function disorder Inferred relationship Existential restriction modifier
Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I Is a True Hereditary platelet function disorder Inferred relationship Existential restriction modifier
Defect of purinergic receptor p2y G protein-coupled 12 Is a True Hereditary platelet function disorder Inferred relationship Existential restriction modifier
Bleeding diathesis due to collagen receptor defect Is a True Hereditary platelet function disorder Inferred relationship Existential restriction modifier
Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder Is a True Hereditary platelet function disorder Inferred relationship Existential restriction modifier
Severe autosomal recessive macrothrombocytopenia Is a True Hereditary platelet function disorder Inferred relationship Existential restriction modifier
Pseudo von Willebrand disease Is a True Hereditary platelet function disorder Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start