Leigh syndrome
Symptom Information:
Symptom ID: | OMIM : No Id available | |||
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Database Frequency: | 7 / 7739 | |||
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All diseases associated with this symptom:
COENZYME Q10 DEFICIENCY, PRIMARY, 3 | (OMIM:614652) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
GRACILE syndrome | (Orphanet:53693) |
Isolated NADH-CoQ reductase deficiency | (Orphanet:2609) |
MEGDEL syndrome | (Orphanet:352328) |
Pyruvate dehydrogenase E3 deficiency | (Orphanet:2394) |