eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | holt oram syndrome |
| Symptom | C0018818|ventricular septal defect |
| Sentences | 1 |
| PubMedID- 20062060 | Mutations are seen in holt-oram syndrome (omim #142900) with atrial and ventricular septal defects, conduction disease, and occasionally af (35). |
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