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74 Possible Causes for 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] The most common complications of transfusional hemochromatosis are hepatic cirrhosis, hypopituitarism, hypogonadism, diabetes mellitus, other endocrinopathies, and cardiomyopathy[ncbi.nlm.nih.gov] Lenihan, Infiltrative Cardiomyopathy and Pericardial Disease, Seminars in Oncology, 40, 2, (199), (2013). Hussam Ghoti, Eliezer A.[doi.org]

  • Propionic Acidemia

    acid synthesis defect with cholestasis and malabsorption Biotin-thiamine-responsive basal ganglia disease Biotinidase deficiency Björnstad syndrome Blue diaper syndrome Brachytelephalangic[se-atlas.de] Cardiomyopathy is a frequent complication in propionic acidemia. It is mostly rapidly fatal and independent of the metabolic control or medical intervention.[ncbi.nlm.nih.gov] Cardiac investigations revealed severe dilated cardiomyopathy (DCM). Biochemical work up led to the diagnosis of PA.[ncbi.nlm.nih.gov]

  • Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1B

    acid synthesis defect with cholestasis and malabsorption Biotin-thiamine-responsive basal ganglia disease Biotinidase deficiency Björnstad syndrome Blue diaper syndrome Brachytelephalangic[se-atlas.de] Emery-Dreifuss muscular dystrophy (EDMD) and limb-girdle muscular dystrophy type 1B (LGMD1B) are characterized by cardiac dysrhythmias, late-onset cardiomyopathy, slowly progressive[ncbi.nlm.nih.gov] LGMD1B is caused by variants in the LMNA gene, and there is considerable phenotypic overlap with the laminopathies, dilated cardiomyopathy and the autosomal dominant form[exeterlaboratory.com]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2R

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] Cardiomyopathy Cardiovascular Cytoskeleton Intermediate Filaments Muscle ARVC Cardiomyopathy Desmin Heart Failure PALM Footnotes 1 Supported by German Ministry of Education[doi.org] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com]

  • Autosomal Dominant 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] cardiomyopathy 7, 2 Nemaline myopathy 4, 5 Tropomyosin Hypertrophic cardiomyopathy 3 Nemaline myopathy 1 Titin Hypertrophic cardiomyopathy 9 Other Fibrillin Marfan syndrome[en.wikipedia.org]

  • Isolated CoQ-Cytochrome C Reductase Deficiency

    acid synthesis defect with cholestasis and malabsorption 0 Blackfan-Diamond disease 0 Breast cancer, familial 0 CACH syndrome 0 COFS syndrome 0 Cardiofaciocutaneous syndrome[research.cchmc.org] Disease Type of connection Histiocytoid cardiomyopathy Leber hereditary optic neuropathy Leigh syndrome with nephrotic syndrome Björnstad syndrome GRACILE syndrome Renal tubulopathy[csbg.cnb.csic.es] MATERNALLY-INHERITED CARDIOMYOPATHY AND HEARING LOSS Is also known as maternally-inherited cardiomyopathy and deafness; trna-lys-related cardiomyopathy-hearing loss syndrome[mendelian.co]

  • 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] Found in patients with CHF, constrictive pericarditis, or restrictive cardiomyopathy.[med-ed.virginia.edu]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2N

    acid synthesis defect with cholestasis and malabsorption Biotin-thiamine-responsive basal ganglia disease Biotinidase deficiency Björnstad syndrome Blue diaper syndrome Brachytelephalangic[se-atlas.de] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com] Cardiomyopathy, familial hypertrophic (CAV3) Dilated cardiomyopathy, 1I (DES) Cardiomyopathy, dilated, 3B, X-linked (DMD) Cardiomyopathy, familial hypertrophic, 1 (MYH7)[meduniwien.ac.at]

  • 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] Associated with more severe cardiomyopathy Progression: Slow Exercise intolerance (50%) Fatigue & Myalgia: Occasional patient Muscle hypertrophy : Calves Rhabdomyolysis :[neuromuscular.wustl.edu] […] disease of heart • • • Back to: « Glycogen storage diseases • • • Types of this condition: 2 Types of glycogen storage diseases : Danon disease Fatal congenital hypertrophic cardiomyopathy[familydiagnosis.com]

  • Congenital Muscular Dystrophy Type 1D

    acid synthesis defect with cholestasis and malabsorption Biotin-thiamine-responsive basal ganglia disease Biotinidase deficiency Björnstad syndrome Blue diaper syndrome Brachytelephalangic[se-atlas.de] Among the nonspecified dystroglycanopathies, CI manifests as dilated cardiomyopathy, hypertrophic cardiomyopathy (CMP) or systolic dysfunction.[pediatrics.aappublications.org] FKTN MDDGA4, MDDGB4, MDDGC4 (LGMD2M), dilated cardiomyopathy GAA glycogen storage disease-2 (Pompe disease) GMPPB MDDGA14, MDDGB14, MDDGC14 (LGMD2T) HNRNPDL * LGMD1G ISPD[invitae.com]

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