1208726006: Fever-associated acute infantile liver failure syndrome (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Viscus structure finding (finding)\Liver finding\Disease of liver\Hepatic failure\Acute hepatic failure\Fever-associated acute infantile liver failure syndrome (disorder)
• \Finding of trunk structure\Liver finding\Disease of liver\Hepatic failure\Acute hepatic failure\Fever-associated acute infantile liver failure syndrome (disorder)
• \Finding of trunk structure\Disorder of trunk (disorder)\Disease of liver\Hepatic failure\Acute hepatic failure\Fever-associated acute infantile liver failure syndrome (disorder)
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Fever-associated acute infantile liver failure syndrome (disorder)
• \Disease\Disorder of body system\Disease of liver\Hepatic failure\Acute hepatic failure\Fever-associated acute infantile liver failure syndrome (disorder)
• \Disease\Disorder of trunk (disorder)\Disease of liver\Hepatic failure\Acute hepatic failure\Fever-associated acute infantile liver failure syndrome (disorder)

Status: current. Date: 31-Mar 2022

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4970639010	Fever-associated acute infantile liver failure syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4970640012	Fever-associated acute infantile liver failure syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4970641011	A rare genetic parenchymatous liver disease with characteristics of infantile or early childhood onset of recurrent episodes of acute liver failure precipitated by a febrile illness. During the life-threatening episodes, patients present with vomiting, lethargy, jaundice as well as elevated levels of liver enzymes and coagulopathy. There is usually complete recovery between the episodes with conservative treatment.	en	Definition	Inactive	Entire term case sensitive (core metadata concept)	SNOMED CT core
5399862011	A rare genetic parenchymatous liver disease characterized by infantile or early childhood onset of recurrent episodes of acute liver failure precipitated by a febrile illness. During the life-threatening episodes, patients present with vomiting, lethargy, jaundice, as well as elevated levels of liver enzymes and coagulopathy. There is usually complete recovery between the episodes with conservative treatment.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5399863018	A rare genetic parenchymatous liver disease characterised by infantile or early childhood onset of recurrent episodes of acute liver failure precipitated by a febrile illness. During the life-threatening episodes, patients present with vomiting, lethargy, jaundice, as well as elevated levels of liver enzymes and coagulopathy. There is usually complete recovery between the episodes with conservative treatment.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Congenital syphilitic hepatomegaly

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