PedAM
Pediatric Disease Annotations & Medicines
| Disease | cardiomyopathy |
| Phenotype | C0162666|mitochondrial encephalomyopathy |
| Sentences | 1 |
| PubMedID- 26124772 | Mitochondrial dysfunctions caused by respiratory chain complex i deficiency have been shown to possibly originate from deleterious mutations in either the nuclear or the mitochondrial genomes, resulting in a wide spectrum of human diseases ranging from leber hereditary optic neuropathy (lhon), that specifically targets one organ, to diseases affecting several organs as the mitochondrial encephalomyopathy associated with cardiomyopathy (fassone and rahman, 2012). |
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