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90 Possible Causes for Cardiomyopathy, Green Jaundice, Hemochromatosis

  • Hemochromatosis

    Hemochromatosis usually occurs in men above the age of 50 years.[symptoma.com] […] or odd colored skin (ashen gray green or reddish) • Abdominal pain (upper right quadrant—in area of the liver) • Joint pain • Rapid weight loss • Gall bladder, pancreas or[irondisorders.org] The most common complications of transfusional hemochromatosis are hepatic cirrhosis, hypopituitarism, hypogonadism, diabetes mellitus, other endocrinopathies, and cardiomyopathy[ncbi.nlm.nih.gov]

  • Passive Congestion of the Liver

    Kayser-Fleischer ring—brown-green ring of copper deposit around the cornea, pathognomonic for Wilson’s disease Nail changes: Muehrcke’s nails—paired horizontal white bands[aafp.org] […] fibrosing cardiomyopathy (idiopathic cardiomyopathy, interstitial myocardial fibrosis) most frequently diagnosed; develops secondary to hypertension in lowland gorillas,[askjpc.org] Liver cancer Inherited diseases, such as hemochromatosis and Wilson disease Symptoms of liver disease can vary, but they often include swelling of the abdomen and legs, bruising[icdlist.com]

  • Portal Cirrhosis

    Kayser-Fleischer ring—brown-green ring of copper deposit around the cornea, pathognomonic for Wilson’s disease Nail changes: Muehrcke’s nails—paired horizontal white bands[aafp.org] Authors : Lupu, Diana Laura 1 Subjects: * CARDIOVASCULAR diseases ; * CIRRHOSIS of the liver ; * CARDIOMYOPATHIES Source: Romanian Medical Journal. 2010, Vol. 57 Issue 1,[library.rangercollege.edu] Wilson disease, hemochromatosis and other rare inherited liver diseases.[singhealth.com.sg]

  • Microcephalic Primordial Dwarfism due to ZNF335 Deficiency

    […] to 21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1-SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] , Dilated, 1ee MYH6 Cardiomyopathy, Dilated, 1g TTN Cardiomyopathy, Dilated, 1y TPM1 Cardiomyopathy, Familial Hypertrophic, 1 MYH6 Cardiomyopathy, Familial Hypertrophic, 14[selfdecode.com] Hyperbiliverdinemia, 614156 (3) BLVRB G:600941 . . BLZF1 G:608692 . . BMF G:606266 . . BMI1 G:164831 . . BMIQ1 P:606641 . . BMIQ2 P:606643 . . BMIQ3 P:607446 . .[usegalaxy.org]

  • 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] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com] Type 1 7 Hemochromatosis Type 2 2 Hemochromatosis Type 2B 2 Hemochromatosis Type 3 2 Hemochromatosis Type 4 2 Hemochromatosis Type 5 1 Hemoglobin H Disease 2 Hemolytic anemia[preventiongenetics.com]

  • Primary Hemochromatosis Type 1

    […] or odd colored skin (ashen gray green or reddish) • Abdominal pain (upper right quadrant—in area of the liver) • Joint pain • Rapid weight loss • Gall bladder, pancreas or[irondisorders.org] Iron overload can cause hepatic cirrhosis, hepatocellular carcinoma, diabetes mellitus, arthropathy, and cardiomyopathy.[mayomedicallaboratories.com] Type 1 hemochromatosis is also commonly referred to as hereditary hemochromatosis or genetic hemochromatosis.[hemochromatosishelp.com]

  • Porphyria

    ., and Thomson S. ( 1948 ) A case of chronic porphyria associated with recurrent jaundice. Quarterly Journal of Medicine 51: 123 - 137.[doi.org] Cardiomyopathy can occur in Refsum disease owing to phytanic acid storage and in acute porphyric crises owing to electrolyte disturbance (in as many as 25% of acute intermittent[web.archive.org] […] associated with a combination of multiple susceptibility factors such as alcohol use, smoking, hepatitis C virus infection, HIV infection, estrogen use, and mutations of the hemochromatosis[ncbi.nlm.nih.gov]

  • Hypertrichotic Osteochondrodysplasia

    235200 HFE hemochromatosis Hemoglobin H disease, nondeletional 613978 HBA2 hemoglobin, alpha 2 Hemophilia Hemophilia A 306700 F8 coagulation factor VIII, procoagulant component[ac-gen.com] Cases 401948 Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency 4 Cases 168588 Hyperandrogenism due to cortisone reductase deficiency 11 Cases 276405 Hyperbiliverdinemia[azkurs.org] Diseases related with Cardiomyopathy and Short phalanx of finger In the following list you will find some of the most common rare diseases related to Cardiomyopathy and Short[mendelian.co]

  • Chronic Liver Disease

    Kayser-Fleischer ring—brown-green ring of copper deposit around the cornea, pathognomonic for Wilson’s disease Nail changes: Muehrcke’s nails—paired horizontal white bands[aafp.org] […] venesection or desferrioxamine Wilson’s Autosomal recessive disorder leading to copper accumulation Leads to liver cirrhosis, neuropsychiatric symptoms including parkinsonism, cardiomyopathy[oxfordmedicaleducation.com] One involves hemochromatosis.[gastroenterologyandhepatology.net]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    Hyperbiliverdinemia, 614156 (3) BLVRB G:600941 . . BLZF1 G:608692 . . BMF G:606266 . . BMI1 G:164831 . . BMIQ1 P:606641 . . BMIQ2 P:606643 . . BMIQ3 P:607446 . .[usegalaxy.org] 1A Dilated cardiomyopathy 1A Dilated cardiomyopathy 1AA Dilated cardiomyopathy 1BB Dilated cardiomyopathy 1C Dilated cardiomyopathy 1D Dilated cardiomyopathy 1E Dilated cardiomyopathy[pentacorelab.hu] Hemochromatosis, Type 2A Hemochromatosis, Type 3 Hemochromatosis, Type 4 Hemolytic Anemia Hemolytic Anemia due to Adenylate Kinase Deficiency Hemolytic Anemia due to Glutathione[sequencing.com]

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