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Results 1 - 10 of 14 for Myopathy diabetes mellitus
  1. MT-TE gene 
    ... and deafness (MIDD). People with this condition have diabetes and sometimes hearing loss, particularly of high tones. Affected individuals may also have muscle weakness (myopathy) and problems with their eyes, heart, or kidneys. ...
    https://medlineplus.gov/genetics/gene/mt-te - Genetics
  2. MT-TL1 gene 
    ... this syndrome include muscle twitches (myoclonus), muscle weakness (myopathy), difficulty coordinating movement (ataxia), hearing loss, seizures, and diabetes.Mutations that cause MERRF/MELAS overlap syndrome each ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  3. Neutral lipid storage disease with myopathy 
    ... type 2 diabetes (the most common form of diabetes). Signs and symptoms of neutral lipid storage disease with myopathy vary greatly among affected individuals. Neutral lipid storage ...
    https://medlineplus.gov/...utral-lipid-storage-disease-with-myopathy - Genetics
  4. HLA-DQA1 gene 
    ... Condition MedlinePlus Genetics provides information about ... other HLA genes affect the risk of type 1 diabetes. Type 1 diabetes is characterized by high blood ...
    https://medlineplus.gov/genetics/gene/hla-dqa1 - Genetics
  5. PTPN22 gene 
    ... Condition MedlinePlus Genetics provides information about Idiopathic ... diabetes More About This Health Condition Studies have associated ...
    https://medlineplus.gov/genetics/gene/ptpn22 - Genetics
  6. Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes 
    ... the brain and nervous system (encephalo-) and muscles (myopathy). The signs and symptoms of this disorder most ... family history of MELAS. MELAS MELAS syndrome Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes Mitochondrial ...
    https://medlineplus.gov/...-lactic-acidosis-and-stroke-like-episodes - Genetics
  7. HLA-DRB1 gene 
    ... Eisenbarth GS. Extreme genetic risk for type 1A diabetes. Proc Natl Acad Sci ... myopathies: major histocompatibility complex and beyond. Curr Opin Rheumatol. ...
    https://medlineplus.gov/genetics/gene/hla-drb1 - Genetics
  8. Myotonic dystrophy 
    ... Myotonic dystrophy type 2 Myotonic dystrophy Proximal myotonic myopathy Steinert myotonic dystrophy National Organization for Rare Disorders ( ...
    https://medlineplus.gov/genetics/condition/myotonic-dystrophy - Genetics
  9. MT-TK gene 
    ... this syndrome include recurrent severe headaches, muscle weakness (myopathy), difficulty coordinating movements (ataxia), hearing loss, and stroke- ... early childhood and include vomiting, seizures, delayed development, myopathy, and problems with movement. Heart disease, kidney problems, ...
    https://medlineplus.gov/genetics/gene/mt-tk - Genetics
  10. Mitochondrial DNA 
    ... the condition is usually characterized by muscle weakness (myopathy) and pain, especially during exercise (exercise intolerance). More ... features include muscle weakness and wasting, movement problems, diabetes, kidney failure, heart disease, loss of intellectual functions ( ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
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