eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | citrullinemia |
| Symptom | C0019151|hepatic encephalopathy |
| Sentences | 1 |
| PubMedID- 20118603 | Citrin deficiency caused by slc25a13 gene mutations develops into adult-onset type ii citrullinemia (ctln2) presenting with hepatic encephalopathy. |
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