eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | cerebellar ataxia |
| Comorbidity | C0796074|mohr-tranebjaerg syndrome |
| Sentences | 1 |
| PubMedID- 22335339 | Among syndromic mids due to nuclear dna (ndna) mutations, cognitive decline has been reported in myo-neuro-gastro-intestinal encephalopathy, mitochondrial recessive ataxia syndrome, spinocerebellar ataxia with encephalopathy, mohr-tranebjaerg syndrome, leuko-encephalopathy; brain and spinal cord involvement and lactic acidosis, cmt2, wolfram syndrome, wolf-hirschhorn syndrome and leigh syndrome. |
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