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Results 1 - 10 of 57 for Dilated "Cardiomyopathy," Recessive
  1. DOLK-congenital disorder of glycosylation 
    ... L, Kapusta L, Mandel H, Wevers RA. Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan ...
    https://medlineplus.gov/...dolk-congenital-disorder-of-glycosylation - Genetics
  2. Early-onset myopathy with fatal cardiomyopathy 
    ... of EOMFC, including skeletal muscle weakness and dilated cardiomyopathy. TTN This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ...
    https://medlineplus.gov/...-onset-myopathy-with-fatal-cardiomyopathy - Genetics
  3. JUP gene 
    ... W, Toutouzas P. Genotype-phenotype assessment in autosomal recessive arrhythmogenic right ventricular cardiomyopathy (Naxos disease) caused by a deletion in plakoglobin. ...
    https://medlineplus.gov/genetics/gene/jup - Genetics
  4. Keratoderma with woolly hair 
    ... Whittock N, Leigh IM, Stevens HP, Kelsell DP. Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma. Hum Mol Genet. 2000 ...
    https://medlineplus.gov/.../condition/keratoderma-with-woolly-hair - Genetics
  5. SLC25A4 gene 
    ... weakness of the muscles used for movement, and cardiomyopathy is a thickening of the heart muscle that forces the heart to work harder to pump blood. This disorder is inherited in an autosomal recessive pattern, which means both copies of the SLC25A4 ...
    https://medlineplus.gov/genetics/gene/slc25a4 - Genetics
  6. DSP gene 
    ... Whittock N, Leigh IM, Stevens HP, Kelsell DP. Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma. Hum Mol Genet. 2000 ...
    https://medlineplus.gov/genetics/gene/dsp - Genetics
  7. Dilated cardiomyopathy with ataxia syndrome 
    ... mutation of mitochondrial DNAJC19 causing dilated and noncompaction ... recessive dilated cardiomyopathic syndrome due to defective importation of ...
    https://medlineplus.gov/...lated-cardiomyopathy-with-ataxia-syndrome - Genetics
  8. Malonyl-CoA decarboxylase deficiency 
    ... characteristic features of this disorder including hypoglycemia and cardiomyopathy. Byproducts of fatty acid processing ... This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ...
    https://medlineplus.gov/.../malonyl-coa-decarboxylase-deficiency - Genetics
  9. Familial dilated cardiomyopathy 
    ... altered gene never develop features of familial dilated cardiomyopathy. (This ... in an autosomal recessive pattern, which means both copies of the gene ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  10. SGCD gene 
    ... copies of the gene in each cell (autosomal recessive inheritance pattern).A small number of people with limb-girdle muscular dystrophy type 2F have developed a heart condition called dilated cardiomyopathy. Dilated cardiomyopathy is a form of heart disease ...
    https://medlineplus.gov/genetics/gene/sgcd - Genetics
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