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Results 1 - 10 of 12 for Familial isolated dilated cardiomyopathy
  1. Familial dilated cardiomyopathy 
    ... of the condition in these individuals is unknown.Familial dilated cardiomyopathy is described as nonsyndromic or isolated because it typically affects only the heart. However, ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  2. Rippling muscle disease 
    ... CAV3-related distal myopathy, limb-girdle muscular dystrophy, isolated ... within the same family.Some people with rippling muscle disease do not ...
    https://medlineplus.gov/genetics/condition/rippling-muscle-disease - Genetics
  3. CAV3-related distal myopathy 
    ... including limb-girdle muscular dystrophy, rippling muscle disease, isolated hyperCKemia, and a heart disorder ... This condition is inherited in an autosomal ...
    https://medlineplus.gov/.../condition/cav3-related-distal-myopathy - Genetics
  4. Isolated hyperCKemia 
    ... kinase that characterize this condition.In addition to isolated hyperCKemia, CAV3 gene mutations can ... This condition is inherited in an autosomal ...
    https://medlineplus.gov/genetics/condition/isolated-hyperckemia - Genetics
  5. CAV3 gene 
    ... failure.When caused by CAV3 gene mutations, hypertrophic cardiomyopathy as well ... even within the same family.Mutations in the CAV3 gene have also been ...
    https://medlineplus.gov/genetics/gene/cav3 - Genetics
  6. TAFAZZIN gene 
    ... This Health Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/tafazzin - Genetics
  7. Left ventricular noncompaction 
    ... their sons. Fetal myocardium Honeycomb myocardium Hypertrabeculation syndrome Isolated noncompaction of the ventricular myocardium Left ventricular hypertrabeculation Left ventricular myocardial noncompaction cardiomyopathy Left ventricular non-compaction LVHT LVNC Non-compaction ...
    https://medlineplus.gov/.../condition/left-ventricular-noncompaction - Genetics
  8. ACAD9 deficiency 
    ... dehydrogenase 9 deficiency Deficiency of acyl-CoA dehydrogenase family member 9 Mitochondrial complex I deficiency due to ACAD9 deficiency Genetic Testing Registry: Acyl-CoA dehydrogenase 9 deficiency Isolated complex I deficiency National Organization for Rare Disorders ( ...
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics
  9. Mitochondrial complex III deficiency 
    ... disorders can appear in every generation of a family and can affect both males and females, but fathers do not pass traits associated with changes in mtDNA to their children. Isolated CoQ-cytochrome c reductase deficiency Ubiquinone-cytochrome c ...
    https://medlineplus.gov/.../mitochondrial-complex-iii-deficiency - Genetics
  10. Mitochondrial complex V deficiency 
    ... disorders can appear in every generation of a family and can affect both males and females, but fathers do not pass traits associated with ... ATP synthase deficiency National Organization for Rare Disorders ( ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
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