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117 Possible Causes for Anemia, Cardiomyopathy, Green Jaundice

  • Hemochromatosis

    […] 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] We present the case of 17 years old girl with congenital hypoplastic anemia and multihormonal insufficiency due to secondary hemochromatosis.[ncbi.nlm.nih.gov] Lenihan, Infiltrative Cardiomyopathy and Pericardial Disease, Seminars in Oncology, 40, 2, (199), (2013). Hussam Ghoti, Eliezer A.[doi.org]

  • 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]

  • Waters-West Syndrome

    21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1- SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] MalaCards based summary : Hemolytic Anemia, Lethal Congenital Nonspherocytic, with Genital and Other Abnormalities, is also known as hemolytic anemia lethal congenital nonspherocytic[malacards.org] 1A 6 Dilated Cardiomyopathy 1Aa 6 Dilated Cardiomyopathy 1BB 1 Dilated Cardiomyopathy 1C 6 Dilated Cardiomyopathy 1CC 6 Dilated Cardiomyopathy 1D 4 Dilated Cardiomyopathy[preventiongenetics.com]

  • 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] 1 Diamond-Blackfan anemia 10 Diamond-Blackfan anemia 3 Diamond-Blackfan anemia 5 Diamond-Blackfan anemia 7 Diamond-Blackfan anemia 8 Diamond-Blackfan anemia 9 Diffuse mesangial[pentacorelab.hu] , Complementation Group A Fanconi Anemia, Complementation Group C Fanconi Anemia, Complementation Group D1 Fanconi Anemia, Complementation Group E Fanconi Anemia, Complementation[sequencing.com]

  • Glycogen Storage Disease due to Muscle Beta-Enolase Deficiency

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] RBC glycogen levels/structure: inc. amount; normal structure Clinical Sx: Type VII (Tarui Dz) Exercise intolerance similar to Type V, but may alsopresent with hemolytic anemia[quizlet.com] Associated with more severe cardiomyopathy Progression: Slow Exercise intolerance (50%) Fatigue & Myalgia: Occasional patient Muscle hypertrophy : Calves Rhabdomyolysis :[neuromuscular.wustl.edu]

  • 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] Various disorders of the hepatobiliary system can occur due to sickling in patients with sickle cell anemia.[ncbi.nlm.nih.gov] […] venesection or desferrioxamine Wilson’s Autosomal recessive disorder leading to copper accumulation Leads to liver cirrhosis, neuropsychiatric symptoms including parkinsonism, cardiomyopathy[oxfordmedicaleducation.com]

  • Primary Biliary Cirrhosis

    Perera DR, Greene ML, Fenster F: Cholestasis associated with extrabiliary Hodgkin's disease. Gastroenterology 1974;67:680–685.[clevelandclinicmeded.com] Autoimmune hepatitis (AIH) and primary biliary cirrhosis (PBC) associated with Evans syndrome; combination of autoimmune hemolytic anemia (AIHA) and immune thrombocytopenic[ncbi.nlm.nih.gov] In 1993 Varga and co-workers described two cases of asymptomatic PBC with a syndrome of severe progressive myopathy, cardiomyopathy, and gastrointestinal dysmotility.[scielo.br]

  • 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] 1 2 Diamond-Blackfan Anemia 10 2 Diamond-Blackfan Anemia 11 2 Diamond-Blackfan Anemia 12 2 Diamond-Blackfan Anemia 3 2 Diamond-Blackfan Anemia 4 2 Diamond-Blackfan Anemia[preventiongenetics.com] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com]

  • Hypertrichotic Osteochondrodysplasia

    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] […] block, progressive, type IA 113900 SCN5A sodium channel, voltage-gated, type V, alpha subunit Heart-hand syndrome, Slovenian type 610140 LMNA lamin A/C Heinz body Heinz body anemia[ac-gen.com] 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]

  • Thallium Poisoning

    Urine may have a slight green discoloration. Hepatic failure or jaundice occurs in extreme cases.[calpoison.org] […] patient was diagnosed with toxic encephalopathy induced by thallium poisoning; in addition, she was also diagnosed with bilateral pneumonia, respiratory failure, moderate anemia[ncbi.nlm.nih.gov] Individuals with severe inorganic arsenic poisoning may experience heart problems (cardiomyopathy); accumulation of acid in the tubes of the kidneys (renal tubular acidosis[rarediseases.org]

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