The search resulted in 17 diseases.
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| 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 |