PedAM
Pediatric Disease Annotations & Medicines
| Disease | intellectual disability |
| Phenotype | C0037773|hereditary spastic paraplegia |
| Sentences | 1 |
| PubMedID- 26113134 | Truncating mutation in intracellular phospholipase a(1) gene (ddhd2) in hereditary spastic paraplegia with intellectual disability (spg54). |
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