eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | barth syndrome |
| Symptom | C0007193|dilated cardiomyopathy |
| Sentences | 1 |
| PubMedID- 23031367 | Intrafamilial variability for novel taz gene mutation: barth syndrome with dilated cardiomyopathy and heart failure in an infant and left ventricular noncompaction in his great-uncle. |
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