All diseases

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ID     

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Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01957 HML myopathy with lactic acidosis, hereditary (HML) 255125 AR 22 20 ISCU - muscular disorder characterized by childhood onset of exercise intolerance with muscle tenderness, cramping, dyspnea, palpitations; biochemical features include lactic acidosis and (rarely) rhabdomyolysis; chronic disorder with remission and exacerbation of muscle phenotype
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