ONKI3 | Medical Subject Headings


Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Fetal Diseases ∟ Erythroblastosis, Fetal ∟ Kernicterus 10 coordinate concepts ∟ Brain Diseases, Metabolic, Inborn \| ∟ Hepatic Encephalopathy \| ∟ Mitochondrial Encephalomyopathies \| ∟ Myelinolysis, Central Pontine \| ∟ Reye Syndrome \| ∟ Wernicke Encephalopathy \| ∟ Hydrops Fetalis \| ∟ D006932Q000151* \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Jaundice Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Erythroblastosis, Fetal ∟ Kernicterus 10 coordinate concepts ∟ Brain Diseases, Metabolic, Inborn \| ∟ Hepatic Encephalopathy \| ∟ Mitochondrial Encephalomyopathies \| ∟ Myelinolysis, Central Pontine \| ∟ Reye Syndrome \| ∟ Wernicke Encephalopathy \| ∟ Hydrops Fetalis \| ∟ D006932Q000151* \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Jaundice Medical Subject Headings (MeSH) ∟ Female Urogenital Diseases and Pregnancy Complications ∟ Pregnancy Complications ∟ Fetal Diseases ∟ Erythroblastosis, Fetal ∟ Kernicterus 10 coordinate concepts ∟ Brain Diseases, Metabolic, Inborn \| ∟ Hepatic Encephalopathy \| ∟ Mitochondrial Encephalomyopathies \| ∟ Myelinolysis, Central Pontine \| ∟ Reye Syndrome \| ∟ Wernicke Encephalopathy \| ∟ Hydrops Fetalis \| ∟ D006932Q000151* \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Jaundice Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Group Incompatibility ∟ Erythroblastosis, Fetal ∟ Kernicterus 10 coordinate concepts ∟ Brain Diseases, Metabolic, Inborn \| ∟ Hepatic Encephalopathy \| ∟ Mitochondrial Encephalomyopathies \| ∟ Myelinolysis, Central Pontine \| ∟ Reye Syndrome \| ∟ Wernicke Encephalopathy \| ∟ Hydrops Fetalis \| ∟ D006932Q000151* \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Jaundice Medical Subject Headings (MeSH) ∟ Immune System Diseases ∟ Blood Group Incompatibility ∟ Erythroblastosis, Fetal ∟ Kernicterus 10 coordinate concepts ∟ Brain Diseases, Metabolic, Inborn \| ∟ Hepatic Encephalopathy \| ∟ Mitochondrial Encephalomyopathies \| ∟ Myelinolysis, Central Pontine \| ∟ Reye Syndrome \| ∟ Wernicke Encephalopathy \| ∟ Hydrops Fetalis \| ∟ D006932Q000151* \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Jaundice Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Brain Diseases, Metabolic ∟ Kernicterus 10 coordinate concepts ∟ Brain Diseases, Metabolic, Inborn \| ∟ Hepatic Encephalopathy \| ∟ Mitochondrial Encephalomyopathies \| ∟ Myelinolysis, Central Pontine \| ∟ Reye Syndrome \| ∟ Wernicke Encephalopathy \| ∟ Hydrops Fetalis \| ∟ D006932Q000151* \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Jaundice Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Brain Diseases, Metabolic ∟ Kernicterus 10 coordinate concepts ∟ Brain Diseases, Metabolic, Inborn \| ∟ Hepatic Encephalopathy \| ∟ Mitochondrial Encephalomyopathies \| ∟ Myelinolysis, Central Pontine \| ∟ Reye Syndrome \| ∟ Wernicke Encephalopathy \| ∟ Hydrops Fetalis \| ∟ D006932Q000151* \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Jaundice Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Hyperbilirubinemia ∟ Kernicterus 10 coordinate concepts ∟ Brain Diseases, Metabolic, Inborn \| ∟ Hepatic Encephalopathy \| ∟ Mitochondrial Encephalomyopathies \| ∟ Myelinolysis, Central Pontine \| ∟ Reye Syndrome \| ∟ Wernicke Encephalopathy \| ∟ Hydrops Fetalis \| ∟ D006932Q000151* \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Jaundice X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Fetal Diseases ∟ Erythroblastosis, Fetal ∟ Kernicterus Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Erythroblastosis, Fetal ∟ Kernicterus Medical Subject Headings (MeSH) ∟ Female Urogenital Diseases and Pregnancy Complications ∟ Pregnancy Complications ∟ Fetal Diseases ∟ Erythroblastosis, Fetal ∟ Kernicterus Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Group Incompatibility ∟ Erythroblastosis, Fetal ∟ Kernicterus Medical Subject Headings (MeSH) ∟ Immune System Diseases ∟ Blood Group Incompatibility ∟ Erythroblastosis, Fetal ∟ Kernicterus Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Brain Diseases, Metabolic ∟ Kernicterus Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Brain Diseases, Metabolic ∟ Kernicterus Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Hyperbilirubinemia ∟ Kernicterus Erythroblastosis, Fetal > Fetal Diseases > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Erythroblastosis, Fetal > Infant, Newborn, Diseases > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Erythroblastosis, Fetal > Fetal Diseases > Pregnancy Complications > Female Urogenital Diseases and Pregnancy Complications > Medical Subject Headings (MeSH) Erythroblastosis, Fetal > Blood Group Incompatibility > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Erythroblastosis, Fetal > Blood Group Incompatibility > Immune System Diseases > Medical Subject Headings (MeSH) Brain Diseases, Metabolic > Brain Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Brain Diseases, Metabolic > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Hyperbilirubinemia > Pathologic Processes > Pathological Conditions, Signs and Symptoms > Medical Subject Headings (MeSH) X
Scope note:	A term used pathologically to describe BILIRUBIN staining of the BASAL GANGLIA; BRAIN STEM; and CEREBELLUM and clinically to describe a syndrome associated with HYPERBILIRUBINEMIA. Clinical features include athetosis, MUSCLE SPASTICITY or hypotonia, impaired vertical gaze, and DEAFNESS. Nonconjugated bilirubin enters the brain and acts as a neurotoxin, often in association with conditions that impair the BLOOD-BRAIN BARRIER (e.g., SEPSIS). This condition occurs primarily in neonates (INFANT, NEWBORN), but may rarely occur in adults. (Menkes, Textbook of Child Neurology, 5th ed, p613) X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Brain Diseases, Metabolic, Inborn \| Hepatic Encephalopathy \| Mitochondrial Encephalomyopathies \| Myelinolysis, Central Pontine \| Reye Syndrome \| Wernicke Encephalopathy \| Hydrops Fetalis \| D006932Q000151* \| Hyperbilirubinemia, Neonatal \| Jaundice X
URI:	X
Labels and equivalent concepts:	Kernikterus (fi) Ikterus, kern- (fi, replaced) Kernikterus (sv) Hyperbilirubinemic Encephalopathy (en, replaced) Encephalopathy, Bilirubin (en, replaced) Encephalopathy, Hyperbilirubinemic (en, replaced) Bilirubin Encephalopathy (en, replaced) Encephalopathia e bilirubino (la-FI, replaced) Icterus nuclearis (la-FI, replaced) Kernicterus (en-FI, replaced) X
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