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Crigler-najjar Syndrome
Crigler-Najjar syndrome
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Related in the Kosmos
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Hepatology
(12)
Conjugated bilirubin
Hyperbilirubinemia
Lucey-Driscoll syndrome
Gilbert syndrome
Dubin-Johnson syndrome
Dubin-Johnson syndrome
Rotor syndrome
Cholestasis
Neonatal jaundice
Liver enzyme
Meckel-Gruber syndrome
Urobilinogen
Liver transplantation
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Inborn errors of metabolism
Glutaricaciduria
Metabolic disorder
Rotor syndrome
Syndromes
(12)
Cutis hyperelastica
Cushings syndrome
Ablepharon macrostomia syndrome
5p deletion syndrome
Craniofacial dysostosis
Craniofacial dysostosis
Kluver Bucy Syndrome
Robinow syndrome
Syndrome
Lucey-Driscoll syndrome
Gilbert syndrome
Dubin-Johnson syndrome
Rotor syndrome
more...
Pediatrics
Shwachman syndrome
Craniosynostosis
Neonatal jaundice
Metabolic disorder
Genetic disorders
(26)
Gunther disease
ALAD porphyria
VATER syndrome
Acrodermatitis enteropathica
Thrombocytopenia absent radius
Thrombocytopenia absent radius
Multiple hereditary exostoses
Popliteal pterygium syndrome
Laurence Moon syndrome
Variegate porphyria
Pallister-Hall syndrome
Hereditary coproporphyria
Kindler syndrome
Costello syndrome
Acute intermittent porphyria
Cutis hyperelastica
Lucey-Driscoll syndrome
Glutaricaciduria
Gilbert syndrome
Dubin-Johnson syndrome
Rotor syndrome
Ablepharon macrostomia syndrome
Shwachman syndrome
5p deletion syndrome
Meckel-Gruber syndrome
Craniofacial dysostosis
Robinow syndrome
more...
Congenital disorders
Corpus callosum agenesis
Cutis hyperelastica
Acrodermatitis enteropathica
Endocrinology
Conns Syndrome
Androblastoma
Cushings syndrome
Porphyrias
(10)
Hepatoeryt- hropoietic porphyria
Porphyria, hepatic
ALAD porphyria
Acute intermittent porphyria
Erythropoietic porphyria
Erythropoietic porphyria
Erythropoietic protoporphyria
Hereditary coproporphyria
Porphyria
Porphyria cutanea tarda
Variegate porphyria
more...
Haemorrhagic and haematological disorders of fetus and newborn
Kernicterus
Haemorrhagic disease of the newborn
Neonatal jaundice
Polycythemia
Diseases and disorders
(59)
Crigler najjar syndrome type 1
Salaam seizures
Mycobacterial
Craniofrontonasal dysplasia
Hereditary hyperbilirubinemia
Hereditary hyperbilirubinemia
Acute cerebellar ataxia
Floating harbor syndrome
Bilirubin encephalopathy
Congenital nonhemolytic jaundice
Chromosome 5p- syndrome
Actinomycosis
Opitz syndrome
X-linked hypophosphatemic rickets
Gonococcal
Coccidioidomycosis
Granulomatous
Pick disease of the brain
Hypersensitivity
dercum disease
Glomerulonephritis
Rare diseases
Astrocytoma
Isaacs syndrome
Cutis hyperelastica
Conns Syndrome
Corpus callosum agenesis
Hyperbilirubinemia
Cushings syndrome
Lucey-Driscoll syndrome
Glutaricaciduria
Gilbert syndrome
Rotor syndrome
Porphyrias
Gunther disease
Cholestasis
Kernicterus
VATER syndrome
Acrodermatitis enteropathica
Thrombocytopenia absent radius
Neonatal jaundice
Hepatoeryt- hropoietic porphyria
Multiple hereditary exostoses
Ablepharon macrostomia syndrome
Shwachman syndrome
5p deletion syndrome
Popliteal pterygium syndrome
Anemia, iron-deficiency
Craniofacial dysostosis
Variegate porphyria
Pallister-Hall syndrome
Autoimmune hepatitis
Metabolic disorder
Cowden syndrome
Hereditary coproporphyria
Ollier disease
Robinow syndrome
Craniosynostosis
Costello syndrome
Acute intermittent porphyria
more...
See also
(20)
Metabolism
Physiologic
Aquarium granuloma
Glucuronos- yltransferase
Bartholin abscess
Bartholin abscess
Heme metabolism intermediates
UGT1A@
Heme
Hemolysis
UDPGT
Phototherapy
Apolipoprotein B deficiency
Enzyme
Enzyme assay
Liver biopsy
Mental confusion
Hallervorden-spatz syndrome
Aortic aneurysm
Cryptogenic fibrosing alveolitis
Amebic liver abscess
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