ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Jaundice, Chronic Idiopathic

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Hyperbilirubinemia, Hereditary ∟ Jaundice, Chronic Idiopathic 2 coordinate concepts ∟ Crigler-Najjar Syndrome \| ∟ Gilbert Disease Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Hyperbilirubinemia, Neonatal ∟ Jaundice, Neonatal ∟ Jaundice, Chronic Idiopathic 2 coordinate concepts ∟ Crigler-Najjar Syndrome \| ∟ Gilbert Disease Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Hyperbilirubinemia, Hereditary ∟ Jaundice, Chronic Idiopathic 2 coordinate concepts ∟ Crigler-Najjar Syndrome \| ∟ Gilbert Disease Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Hyperbilirubinemia ∟ Hyperbilirubinemia, Neonatal ∟ Jaundice, Neonatal ∟ Jaundice, Chronic Idiopathic 2 coordinate concepts ∟ Crigler-Najjar Syndrome \| ∟ Gilbert Disease X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Hyperbilirubinemia, Hereditary ∟ Jaundice, Chronic Idiopathic Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Hyperbilirubinemia, Neonatal ∟ Jaundice, Neonatal ∟ Jaundice, Chronic Idiopathic Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Hyperbilirubinemia, Hereditary ∟ Jaundice, Chronic Idiopathic Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Hyperbilirubinemia ∟ Hyperbilirubinemia, Neonatal ∟ Jaundice, Neonatal ∟ Jaundice, Chronic Idiopathic Hyperbilirubinemia, Hereditary > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Jaundice, Neonatal > Hyperbilirubinemia, Neonatal > Infant, Newborn, Diseases > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Hyperbilirubinemia, Hereditary > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Jaundice, Neonatal > Hyperbilirubinemia, Neonatal > Hyperbilirubinemia > Pathologic Processes > Pathological Conditions, Signs and Symptoms > Medical Subject Headings (MeSH) X
Scope note:	A benign, autosomally recessive inherited hyperbilirubinemia characterized by the presence of a dark pigment in the centrilobular region of the liver cells. There is a functional defect in biliary excretion of bilirubin, cholephilic dyes, and porphyrins. Affected persons may be asymptomatic or have vague constitutional or gastrointestinal symptoms. The liver may be slightly enlarged, and oral and intravenous cholangiography fails to visualize the biliary tract. X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Crigler-Najjar Syndrome \| Gilbert Disease X
URI:	X
Labels and equivalent concepts:	Krooninen idiopaattinen ikterus (fi) Krooninen idiopaattinen keltatauti (fi, replaced) Krooninen idiopaattinen keltaisuus (fi, replaced) Ikterus, krooninen idiopaattinen (fi, replaced) Gulsot, kronisk idiopatisk (sv) Ikterus, kronisk idiopatisk (sv, replaced) Dubin-Johnson Syndrome (en, replaced) X
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