eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | friedreich ataxia |
| Comorbidity | C0020179|huntington\'s disease |
| Sentences | 1 |
| PubMedID- 24653660 | Currently used molecular diagnostics based on dna analysis can identify 9 neurodegenerative diseases, including spinal cerebellar ataxia inherited in an autosomal dominant manner, dentate-rubro-pallido-luysian atrophy, friedreich's disease, ataxia with ocu-lomotorapraxia, huntington's disease, dystonia type 1, wilson's disease, and some cases of parkinson's disease. |
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