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49762007: Hereditary factor XI deficiency disease (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
82886016 Hereditary factor XI deficiency disease en Synonym Active Only initial character case insensitive SNOMED CT core module
82887013 Hemophilia C en Synonym Active Only initial character case insensitive SNOMED CT core module
82888015 Congenital factor XI deficiency disease en Synonym Active Only initial character case insensitive SNOMED CT core module
82889011 Plasma thromboplastin antecedent deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
82890019 PTA deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
82891015 Rosenthal's disease en Synonym Active Entire term case sensitive SNOMED CT core module
495497019 Haemophilia C en Synonym Active Only initial character case insensitive SNOMED CT core module
787476012 Hereditary factor XI deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
1230777015 Factor XI deficiency en Synonym Inactive Only initial character case insensitive SNOMED CT core module
1230778013 Thromboplastin antecedent deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

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 Existential restriction modifier
Hereditary factor XI deficiency disease Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Hereditary factor XI deficiency disease Is a Contact factor deficiency true Inferred relationship Existential restriction modifier
Hereditary factor XI deficiency disease Is a Hemophilia true Inferred relationship Existential restriction modifier
Hereditary factor XI deficiency disease Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Hereditary factor XI deficiency disease Finding site Body system structure false Inferred relationship Existential restriction modifier
Hereditary factor XI deficiency disease Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Hereditary factor XI deficiency disease Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hereditary factor XI deficiency disease Is a Congenital disease true Inferred relationship Existential restriction modifier
Hereditary factor XI deficiency disease Is a Factor XI deficiency true Inferred relationship Existential restriction modifier
Hereditary factor XI deficiency disease Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Hereditary factor XI deficiency disease Interprets Hemostatic function true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Factor XI deficiency, type II Is a True Hereditary factor XI deficiency disease Inferred relationship Existential restriction modifier
Factor XI deficiency, type III Is a True Hereditary factor XI deficiency disease Inferred relationship Existential restriction modifier
Factor XI deficiency, type I Is a True Hereditary factor XI deficiency disease Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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