Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Cardiogenetic disease · Disorder of phospholipids, sphingolipids and fatty acids biosynthesis · Mitochondrial DNA depletion syndrome · Mitochondrial substrate carrier disorder
Sengers syndrome
Congenital cataract - hypertrophic cardiomyopathy - mitochrondrial myopathy (CCM) is a mitochondrial disease characterized by cataracts, hypertrophic cardiomyopathy, muscle weakness and lactic acidosis after exercise.
This condition has no sub-types.