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27503000: Gilbert's syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
46000010 Gilbert's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
46001014 Gilbert-Lereboullet syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
46002019 Familial nonhemolytic bilirubinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46003012 Chronic intermittent juvenile jaundice en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46004018 Constitutional hepatic dysfunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46005017 Cholemia familiaris simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46006016 Familial nonhemolytic jaundice en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46007013 Gilbert's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
46008015 Hereditary nonhemolytic jaundice en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46009011 Benign unconjugated bilirubinemia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46010018 Meulengracht syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
46011019 Low-grade chronic hyperbilirubinemia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46012014 Congenital familial cholemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483557015 Benign unconjugated bilirubinaemia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483558013 Congenital familial cholaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483559017 Cholaemia familiaris simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483560010 Gilbert syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
483561014 Familial nonhaemolytic bilirubinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483562019 Hereditary nonhaemolytic jaundice en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483563012 Familial nonhaemolytic jaundice en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483564018 Low-grade chronic hyperbilirubinaemia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
758078013 Gilbert's syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2920595018 Gilberts syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
46000010 Gilbert's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
46001014 Gilbert-Lereboullet syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
46002019 Familial nonhemolytic bilirubinemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
46002019 Familial nonhemolytic bilirubinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46003012 Chronic intermittent juvenile jaundice en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
46003012 Chronic intermittent juvenile jaundice en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46004018 Constitutional hepatic dysfunction en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
46004018 Constitutional hepatic dysfunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46005017 Cholemia familiaris simplex en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
46005017 Cholemia familiaris simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46006016 Familial nonhemolytic jaundice en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
46006016 Familial nonhemolytic jaundice en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46007013 Gilbert's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
46008015 Hereditary nonhemolytic jaundice en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
46008015 Hereditary nonhemolytic jaundice en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46009011 Benign unconjugated bilirubinemia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
46009011 Benign unconjugated bilirubinemia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46010018 Meulengracht syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
46011019 Low-grade chronic hyperbilirubinemia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
46011019 Low-grade chronic hyperbilirubinemia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46012014 Congenital familial cholemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
46012014 Congenital familial cholemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483557015 Benign unconjugated bilirubinaemia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
483557015 Benign unconjugated bilirubinaemia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483558013 Congenital familial cholaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
483558013 Congenital familial cholaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483559017 Cholaemia familiaris simplex en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
483559017 Cholaemia familiaris simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483560010 Gilbert syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
483561014 Familial nonhaemolytic bilirubinaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
483561014 Familial nonhaemolytic bilirubinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483562019 Hereditary nonhaemolytic jaundice en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
483562019 Hereditary nonhaemolytic jaundice en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483563012 Familial nonhaemolytic jaundice en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
483563012 Familial nonhaemolytic jaundice en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483564018 Low-grade chronic hyperbilirubinaemia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
483564018 Low-grade chronic hyperbilirubinaemia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
758078013 Gilbert's syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
758078013 Gilbert's syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2920595018 Gilberts syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2920595018 Gilberts syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
957681000195115 sindrome di Gilbert it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
873621000195116 Gilbert-Meulengracht-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
873631000195119 Gilbert-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
873641000195110 Icterus juvenilis intermittens de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
873651000195113 Meulengracht-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
873661000195111 Morbus Meulengracht de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
239361000172118 syndrome de Gilbert fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
239361000172118 syndrome de Gilbert fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
957681000195115 sindrome di Gilbert it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
873621000195116 Gilbert-Meulengracht-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
873631000195119 Gilbert-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
873641000195110 Icterus juvenilis intermittens de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
873651000195113 Meulengracht-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
873661000195111 Morbus Meulengracht de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Gilbert's syndrome Is a Hyperbilirubinemia false Inferred relationship Existential restriction modifier (core metadata concept)
Gilbert's syndrome Is a Inherited disorder of bilirubin metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Gilbert's syndrome Is a Congenital anomaly of liver false Inferred relationship Existential restriction modifier (core metadata concept)
Gilbert's syndrome Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Gilbert's syndrome Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Gilbert's syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Gilbert's syndrome Finding site Liver structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Gilbert's syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Gilbert's syndrome Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Dubin-Johnson syndrome Is a False Gilbert's syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal jaundice due to Gilbert's syndrome (finding) Associated with False Gilbert's syndrome Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal jaundice due to Gilbert's syndrome (finding) Due to True Gilbert's syndrome Inferred relationship Existential restriction modifier (core metadata concept) 2

This concept is not in any reference sets

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