Increased serum and CSF lactate
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
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MedDRA: |
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| Database Frequency: | 7 / 7739 | |
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All diseases associated with this symptom:
| Autosomal recessive ataxia due to ubiquinone deficiency | (Orphanet:139485) |
| Combined oxidative phosphorylation defect type 13 | (Orphanet:319514) |
| Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
| Hypotonia-cerebral atrophy-hyperglycinemia syndrome | (Orphanet:363424) |
| LEBER OPTIC ATROPHY AND DYSTONIA | (OMIM:500001) |
| Lethal encephalopathy due to mitochondrial and peroxisomal fission defect | (Orphanet:330050) |
| Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria | (Orphanet:1933) |