FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.1  |  FHIR Version n/a  User: [n/a]

27503000: Gilbert's syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
46000010 Gilbert's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
46001014 Gilbert-Lereboullet syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
46002019 Familial nonhemolytic bilirubinemia en Synonym Active Entire term case insensitive SNOMED CT core module
46003012 Chronic intermittent juvenile jaundice en Synonym Active Entire term case insensitive SNOMED CT core module
46004018 Constitutional hepatic dysfunction en Synonym Active Entire term case insensitive SNOMED CT core module
46005017 Cholemia familiaris simplex en Synonym Active Entire term case insensitive SNOMED CT core module
46006016 Familial nonhemolytic jaundice en Synonym Active Entire term case insensitive SNOMED CT core module
46007013 Gilbert's disease en Synonym Active Entire term case sensitive SNOMED CT core module
46008015 Hereditary nonhemolytic jaundice en Synonym Active Entire term case insensitive SNOMED CT core module
46009011 Benign unconjugated bilirubinemia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
46010018 Meulengracht syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
46011019 Low-grade chronic hyperbilirubinemia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
46012014 Congenital familial cholemia en Synonym Active Entire term case insensitive SNOMED CT core module
483557015 Benign unconjugated bilirubinaemia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
483558013 Congenital familial cholaemia en Synonym Active Entire term case insensitive SNOMED CT core module
483559017 Cholaemia familiaris simplex en Synonym Active Entire term case insensitive SNOMED CT core module
483560010 Gilbert syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
483561014 Familial nonhaemolytic bilirubinaemia en Synonym Active Entire term case insensitive SNOMED CT core module
483562019 Hereditary nonhaemolytic jaundice en Synonym Active Entire term case insensitive SNOMED CT core module
483563012 Familial nonhaemolytic jaundice en Synonym Active Entire term case insensitive SNOMED CT core module
483564018 Low-grade chronic hyperbilirubinaemia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
758078013 Gilbert's syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
2920595018 Gilberts syndrome en Synonym Active Entire term case sensitive SNOMED CT core 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
Gilbert's syndrome Is a Inherited disorder of bilirubin metabolism true Inferred relationship Existential restriction modifier
Gilbert's syndrome Is a Congenital anomaly of liver false Inferred relationship Existential restriction modifier
Gilbert's syndrome Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier
Gilbert's syndrome Finding site Digestive organ structure false Inferred relationship Existential restriction modifier 1
Gilbert's syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Gilbert's syndrome Finding site Liver structure false Inferred relationship Existential restriction modifier
Gilbert's syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Gilbert's syndrome Finding site Body system structure false Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Dubin-Johnson syndrome Is a False Gilbert's syndrome Inferred relationship Existential restriction modifier
Neonatal jaundice with Gilbert's syndrome Associated with True Gilbert's syndrome Inferred relationship Existential restriction modifier 1

This concept is not in any reference sets

Back to Start