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49762007: Hereditary factor XI deficiency disease (disorder)

Status: current, Defined. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1230778013 Thromboplastin antecedent deficiency en Synonym Active Case insensitive SNOMED CT core
495497019 Haemophilia C en Synonym Active Initial character case insensitive SNOMED CT core
787476012 Hereditary factor XI deficiency disease (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
82886016 Hereditary factor XI deficiency disease en Synonym Active Initial character case insensitive SNOMED CT core
82887013 Hemophilia C en Synonym Active Initial character case insensitive SNOMED CT core
82888015 Congenital factor XI deficiency disease en Synonym Active Initial character case insensitive SNOMED CT core
82889011 Plasma thromboplastin antecedent deficiency en Synonym Active Case insensitive SNOMED CT core
82890019 PTA deficiency en Synonym Active Case sensitive SNOMED CT core
82891015 Rosenthal's disease en Synonym Active Case sensitive SNOMED CT core

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary factor XI deficiency disease Has interpretation Abnormal true Inferred relationship Some 2
Hereditary factor XI deficiency disease Interprets Haemostatic function true Inferred relationship Some 2
Hereditary factor XI deficiency disease Is a Hereditary coagulation factor deficiency false Inferred relationship Some
Hereditary factor XI deficiency disease Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Hereditary factor XI deficiency disease Is a Contact factor deficiency true Inferred relationship Some
Hereditary factor XI deficiency disease Is a Haemophilia true Inferred relationship Some
Hereditary factor XI deficiency disease Finding site Body system structure false Inferred relationship Some
Hereditary factor XI deficiency disease Has definitional manifestation Haemostatic system finding false Inferred relationship Some
Hereditary factor XI deficiency disease Finding site Entire haematological system false Inferred relationship Some
Hereditary factor XI deficiency disease Occurrence Congenital true Inferred relationship Some 1
Hereditary factor XI deficiency disease Is a Congenital disease true Inferred relationship Some
Hereditary factor XI deficiency disease Is a Factor XI deficiency true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Factor XI deficiency, type II Is a True Hereditary factor XI deficiency disease Inferred relationship Some
Factor XI deficiency, type III Is a True Hereditary factor XI deficiency disease Inferred relationship Some
Factor XI deficiency, type I Is a True Hereditary factor XI deficiency disease Inferred relationship Some

Reference Sets

Emergency department reference set

Australian emergency department reference set

NSW Emergency Department reference set

Clinical finding foundation reference set

Australian dialect reference set

Emergency department diagnosis reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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