PedAM
Pediatric Disease Annotations & Medicines
| Disease | hyperammonemia |
| Phenotype | C0020459|hyperinsulinism |
| Sentences | 1 |
| PubMedID- 20164212 | Katp channel mutations were most common (15%) followed by glud1 mutations causing hyperinsulinism with hyperammonemia (5.9%), and hnf4a mutations (5%). |
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