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Hyperbilirubinemia
Hyperbilirubinemia
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Hepatology
(18)
Neonatal hyperbilirubinemia
Bilirubin
Icterus
Crigler-najjar syndrome
Lucey-Driscoll syndrome
Lucey-Driscoll syndrome
Dubin-Johnson syndrome
Gilbert syndrome
Rotor syndrome
Cholestasis
Hepatomegaly
Biliary atresia
Alpha 1 antitrypsin deficiency
Primary sclerosing cholangitis
Glycogen storage disease
Hepatobiliary
Urobilinogen
Common bile duct
Liver biopsy
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Gastroenterology
(9)
Fecal elastase
Fecal fat
Icterus
Dubin-Johnson syndrome
Gilbert syndrome
Gilbert syndrome
Cholestasis
Biliary atresia
Alpha 1 antitrypsin deficiency
Primary sclerosing cholangitis
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Digestive system
Hepatic
Icterus
Hepatobiliary
Common bile duct
Diseases and disorders
(45)
Hereditary hyperbilirubinemia
Kernicterus
Hypochondriacal neurosis
Hutchinson incisors
Hyperchylo- micronemia
Hyperchylo- micronemia
Hyperimmunoglobulin E syndrome
Hypolipoproteinemia
Horizontal nystagmus
Horners syndrome
Hypercalciuria
Bilirubin encephalopathy
Chronic idiopathic jaundice
Rh incompatibility
Perinatal period
Landouzy-Dejerine muscular dystrophy
Gunther disease
Lipofuscinoses
Hemolytic anemia
Leukodystrophy metachromatic
Leiomyoma
Acute intermittent porphyria
Louis-bar syndrome
Velamentous cord insertion
Congenital hypotonia
Limb-girdle muscular dystrophies
Lymphoid hypertrophy
Haemorrhagic disease of the newborn
Neonatal herpes simplex
Leukemia, hairy cell
Brachial plexus lesion
Lymphoplasmacytic lymphoma
G6pd deficiency
Hemolytic jaundice
Hepatoeryt- hropoietic porphyria
Lymphadenopathy
Neonatal hyperbilirubinemia
Icterus
Lucey-Driscoll syndrome
Gilbert syndrome
Rotor syndrome
Cholestasis
Biliary atresia
Alpha 1 antitrypsin deficiency
Primary sclerosing cholangitis
Glycogen storage disease
more...
Haemorrhagic and haematological disorders of fetus and newborn
Polycythemia
Neonatal hyperbilirubinemia
Kernicterus
Haemorrhagic disease of the newborn
Pediatrics
(10)
Merconium
Hemolytic disease of the newborn (ABO)
Wilson Mikity syndrome
Cephalhematoma
Neonatal hyperbilirubinemia
Neonatal hyperbilirubinemia
Hyperimmunoglobulin E syndrome
Crigler-najjar syndrome
Rh incompatibility
Biliary atresia
Haemorrhagic disease of the newborn
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Hematology
(12)
Hyperviscosity.
Hemolysis
Exchange transfusion
Coagulopathy
Neonatal hyperbilirubinemia
Neonatal hyperbilirubinemia
Hypolipoproteinemia
Rh incompatibility
Hemolytic disease of the newborn (ABO)
Polycythemia
Hemolytic anemia
Lymphoplasmacytic lymphoma
G6pd deficiency
more...
Porphyrias
(10)
ALAD porphyria
Acute intermittent porphyria
Erythropoietic porphyria
Erythropoietic protoporphyria
Hepatic porphyria
Hepatic porphyria
Hepatoeryt- hropoietic porphyria
Hereditary coproporphyria
Porphyria
Porphyria cutanea tarda
Variegate porphyria
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Respiratory and cardiovascular disorders specific to the perinatal period
Persistent fetal circulation
Infant respiratory distress syndrome
Intrauterine hypoxia
Pneumonia
Transient tachypnea of the newborn
Wilson Mikity syndrome
Symptoms
Hypertrophic scar
Opisthotonus
Yellow skin
Congenital hypotonia
Lymphadenopathy
Bleeding
(9)
Hemolytic disease of the newborn (anti-Kell)
Hemolytic disease of the newborn (anti-RhE)
Hemolytic disease of the newborn (anti-Rhc)
Hydrops fetalis
Rh disease
Rh disease
Vitamin K deficiency
Neonatal jaundice
Kernicterus
Hemolytic disease of the newborn
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See also
(20)
Hypertrigl- yceridemia
Human artificial chromosome
Hyperparat- hyroidism, secondary
Phototherapy
UGT1*1
UGT1*1
UGT1
Lereboullet
A1 broth
CMOAT
Hepatitis
Neonates
Autosomal
Heme metabolism intermediates
Physiologic
ALAD porphyria
Ursodeoxycholic acid
Congenital hypertonia
American Liver Foundation
Bile pigment
Cephalohematoma
more...
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