The information on this page is for informational purposes only and does not constitute medical advice. Consult your genetic counselor or specialist physician for treatment decisions.

MERRF Syndrome

Prevalence: 1/100000
mitochondrial
Official·OMIM:545000Official·ORPHA551

Myoclonic epilepsy and ragged-red fiber myopathy due to MT-TK gene mutations.

Associated Genes

No gene records found associated with this disease.