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74162007: Progressive intrahepatic cholestasis (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
123149016 Progressive intrahepatic cholestasis en Synonym Active Case insensitive SNOMED CT core
123151017 Familial intrahepatic cholestasis en Synonym Active Case insensitive SNOMED CT core
123152012 Fatal intrahepatic cholestasis en Synonym Active Case insensitive SNOMED CT core
4570357019 Progressive familial intrahepatic cholestasis en Synonym Active Case insensitive SNOMED CT core
4570358012 PFIC - progressive familial intrahepatic cholestasis en Synonym Active Case sensitive SNOMED CT core
814631018 Progressive intrahepatic cholestasis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4570359016 A heterogeneous group of autosomal recessive disorders of childhood that disrupt bile formation and present with cholestasis of hepatocellular origin. Three types of PFIC have been identified and are related to mutations in hepatocellular transport system genes involved in bile formation. Main clinical manifestations include cholestasis, pruritus and jaundice. en Definition Active Case sensitive SNOMED CT core


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Progressive intrahepatic cholestasis Clinical course Progressive true Inferred relationship Some 2
Progressive intrahepatic cholestasis Is a Bilirubin metabolism disorder true Inferred relationship Some
Progressive intrahepatic cholestasis Is a Chronic liver disease true Inferred relationship Some
Progressive intrahepatic cholestasis Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Progressive intrahepatic cholestasis Is a Chronic metabolic disorder true Inferred relationship Some
Progressive intrahepatic cholestasis Is a Hepatic porphyria false Inferred relationship Some
Progressive intrahepatic cholestasis Is a Congenital anomaly of digestive system false Inferred relationship Some
Progressive intrahepatic cholestasis Is a Liver disease false Inferred relationship Some
Progressive intrahepatic cholestasis Is a Digestive system hereditary disorder true Inferred relationship Some
Progressive intrahepatic cholestasis Is a Disorder of bilirubin metabolism and excretion false Inferred relationship Some
Progressive intrahepatic cholestasis Is a Congenital anomaly of trunk false Inferred relationship Some
Progressive intrahepatic cholestasis Is a Disorder of biliary tract false Inferred relationship Some
Progressive intrahepatic cholestasis Is a Liver disease false Inferred relationship Some
Progressive intrahepatic cholestasis Finding site Intrahepatic biliary tract structure true Inferred relationship Some 1
Progressive intrahepatic cholestasis Finding site Liver structure false Inferred relationship Some
Progressive intrahepatic cholestasis Occurrence Congenital false Inferred relationship Some
Progressive intrahepatic cholestasis Is a Disorder of bile duct true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Progressive familial intrahepatic cholestasis type 2 Is a True Progressive intrahepatic cholestasis Inferred relationship Some
Progressive familial intrahepatic cholestasis type 1 Is a True Progressive intrahepatic cholestasis Inferred relationship Some
Progressive familial intrahepatic cholestasis type 3 Is a True Progressive intrahepatic cholestasis Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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