The search resulted in 17 diseases.
Orphanet:104 Leber hereditary optic neuropathy
Orphanet:111 Barth syndrome
Orphanet:1349 Maternally-inherited cardiomyopathy and hearing loss
Orphanet:1369 Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome
Orphanet:137675 Histiocytoid cardiomyopathy
Orphanet:289527 Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency
Orphanet:314637 Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
Orphanet:319678 Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
Orphanet:324525 Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation
Orphanet:352563 Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
Orphanet:369913 Combined oxidative phosphorylation defect type 17
Orphanet:480 Kearns-Sayre syndrome
Orphanet:550 MELAS
Orphanet:551 MERRF
Orphanet:91130 Cardiomyopathy-hypotonia-lactic acidosis syndrome
Orphanet:99718 Leber plus disease
Orphanet:99901 Acyl-CoA dehydrogenase 9 deficiency