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 |
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