eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | hereditary motor and sensory neuropathy v |
| Comorbidity | C0000744|familial hypobetalipoproteinemia |
| Sentences | 1 |
| PubMedID- 25769290 | Spg11 mutation in a turkish familial hypobetalipoproteinemia family with hereditary spastic paraplegia. |
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