eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | opitz g/bbb syndrome |
| Comorbidity | C0271694|familial partial lipodystrophy |
| Sentences | 1 |
| PubMedID- 20041886 | Overlapping syndrome with familial partial lipodystrophy, dunnigan variety and cardiomyopathy due to amino-terminal heterozygous missense lamin a/c mutations. |
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