PedAM
Pediatric Disease Annotations & Medicines
| Disease | hypotonia |
| Phenotype | C0020630|hypophosphatasia |
| Sentences | 1 |
| PubMedID- 25885527 | Pigt mutations cause congenital anomalies-seizures-hypotonia type 3, with hypophosphatasia as key feature [44,45]. |
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