PedAM
Pediatric Disease Annotations & Medicines
| Disease | aneurysm |
| Phenotype | C0042373|vascular disorder |
| Sentences | 1 |
| PubMedID- 24442477 | Another set of mutations in encoding contractile proteins in vascular smc, such as acta2 and myh11, has been found to be responsible for isolated familial vascular disorder with ascending aortic aneurysm and dissection [123, 124]. |
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