All diseases

1 entry on 1 page. Showing entry 1.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01957 HML myopathy with lactic acidosis, hereditary (HML) 255125 - 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
Legend   How to query