Congenital cataract - hypertrophic cardiomyopathy - mitochondrial myopathy OMIM:615418 UMLS:C1859317 Congenital cataract - hypertrophic cardiomyopathy - mitochrondrial myopathy (CCM) is a mitochondrial disease (see this term) characterized by cataracts, hypertrophic cardiomyopathy, muscle weakness and lactic acidosis after exercise. Sengers syndrome MESH:C538280 orphanet OMIM:212350 ICD10:Q87.8 Rare genetic developmental defect during embryogenesis Mitochondrial disease with hypertrophic cardiomyopathy Disorder of phospholipids, sphingolipids and fatty acids biosynthesis with skeletal muscle predominant involvement Disorder of energy metabolism Cardiac disease with cataract