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76 Possible Causes for Hyperbiliverdinemia

  • Hereditary North American Indian Childhood Cirrhosis

    Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary North American Indian childhood cirrhosis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de]

  • Transient Familial Neonatal Hyperbilirubinemia

    Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary North American Indian childhood cirrhosis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de]

  • IgG4-Related Hepatopathy

    Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary North American Indian childhood cirrhosis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de]

  • Congenital Enteropathy due to Enteropeptidase Deficiency

    […] syndrome Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary chronic pancreatitis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de]

  • Familial Recurrent Peripheral Facial Palsy

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] […] skin Granulosa cell cancer Granulosa cell malignant tumor Gravidic intrahepatic cholestasis Gray platelet syndrome Grayson-Wilbrandt corneal dystrophy Greenberg dysplasia Green[orpha.net]

  • Granulomatous Mastitis

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] […] skin Granulosa cell cancer Granulosa cell malignant tumor Gravidic intrahepatic cholestasis Gray platelet syndrome Grayson-Wilbrandt corneal dystrophy Greenberg dysplasia Green[orpha.net]

  • Hereditary Hyperekplexia

    Joubert syndrome 17 Cardiac conduction defect, nonspecific Lethal multiple pterygium syndrome Non-small cell lung cancer Acroerythrokeratoderma Renal hypodysplasia/aplasia 2 Hyperbiliverdinemia[amp.pharm.mssm.edu]

  • Gingival Fibromatosis-Progressive Deafness Syndrome

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] […] skin Granulosa cell cancer Granulosa cell malignant tumor Gravidic intrahepatic cholestasis Gray platelet syndrome Grayson-Wilbrandt corneal dystrophy Greenberg dysplasia Green[orpha.net]

  • Neuronal Ceroid Lipofuscinosis

    […] dystrophy type III Granular-lattice corneal dystrophy Granulomatosis with polyangiitis Gravidic intrahepatic cholestasis Gray platelet syndrome Gräsbeck-Imerslund disease Green[csbg.cnb.csic.es] jaundice Greenberg dysplasia Greig cephalopolysyndactyly syndrome Greither disease Grisart-Destrée syndrome Griscelli disease type 1 Griscelli disease type 2 Griscelli disease[csbg.cnb.csic.es] N-acetylglutamate synthetase deficiency Hyperandrogenism due to cortisone reductase deficiency Hyperargininemia Hyperbilirubinemia type 2 Hyperbilirubinemia, Rotor type Hyperbiliverdinemia[csbg.cnb.csic.es]

  • Limb-Girdle Muscular Dystrophy Type 1H

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] […] skin Granulosa cell cancer Granulosa cell malignant tumor Gravidic intrahepatic cholestasis Gray platelet syndrome Grayson-Wilbrandt corneal dystrophy Greenberg dysplasia Green[orpha.net]

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