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91 Possible Causes for Hyperbiliverdinemia, Onset of Muscle Weakness in Fifth Decade

  • 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] Five subjects presented with a slowly progressive proximal muscle weakness, in both upper and lower limbs, with onset during the fourth-fifth decade of life, which fulfilled[moh-it.pure.elsevier.com] Five subjects presented with a slowly progressive proximal muscle weakness, in both upper and lower limbs, with onset during the fourth-fifth decade that fulfilled the consensus[hal.archives-ouvertes.fr]

  • 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]

    Missing: Onset of Muscle Weakness in Fifth Decade
  • 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]

    Missing: Onset of Muscle Weakness in Fifth Decade
  • 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]

    Missing: Onset of Muscle Weakness in Fifth Decade
  • 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]

    Missing: Onset of Muscle Weakness in Fifth Decade
  • 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]

    Missing: Onset of Muscle Weakness in Fifth Decade
  • Gitelman Syndrome

    We report two adult male siblings of Jewish origin with late onset GS, who presented in their fifth decade of life with muscle weakness, hypokalemia, hypomagnesaemia, and[ncbi.nlm.nih.gov]

    Missing: Hyperbiliverdinemia
  • Spinal and Bulbar Muscular Atrophy

    […] of progressive muscle weakness, atrophy, and fasciculations typically in the fourth or fifth decade of life.[mayomedicallaboratories.com] Age at onset is usually in the third to fifth decade of life, but earlier involvement has been reported.[flybase.org] The clinical severity and age at onset can be quite variable, even within families.[mayomedicallaboratories.com]

    Missing: Hyperbiliverdinemia
  • 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]

    Missing: Onset of Muscle Weakness in Fifth Decade
  • 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]

    Missing: Onset of Muscle Weakness in Fifth Decade

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