PedAM
Pediatric Disease Annotations & Medicines
| Disease | hypobetalipoproteinemia |
| Phenotype | C0037773|hereditary spastic paraplegia |
| Sentences | 1 |
| PubMedID- 25769290 | Spg11 mutation in a turkish familial hypobetalipoproteinemia family with hereditary spastic paraplegia. |
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