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49762007: Hereditary factor XI deficiency disease (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module Reference Sets
82886016 Hereditary factor XI deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
82887013 Hemophilia C en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core US English: Acceptable (foundation metadata concept)
82888015 Congenital factor XI deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
82889011 Plasma thromboplastin antecedent deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
82890019 PTA deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
82891015 Rosenthal's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
495497019 Haemophilia C en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
787476012 Hereditary factor XI deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
1230778013 Thromboplastin antecedent deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)

3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
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 Hemophilia true Inferred relationship Some
Hereditary factor XI deficiency disease Finding site Entire hematological system (body structure) false 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 Hemostatic system finding false Inferred relationship Some
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
Hereditary factor XI deficiency disease Occurrence Congenital true Inferred relationship Some 1
Hereditary factor XI deficiency disease Has interpretation Abnormal true Inferred relationship Some 2
Hereditary factor XI deficiency disease Interprets Hemostatic function true Inferred relationship Some 2

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

GB English

US English

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