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| Term | Meester-Loeys syndrome | ID (Ontology) | DOID:0111861 (Human Disease) |
| Definition | A syndrome characterized by early-onset aortic aneurysm and dissection in hemizygous males and variable presentation from unaffected to fatal aortic dissection in heterozygous females, as well as facial dysmorphism, connective tissue anomalies, and features of Loeys-Dietz syndrome that has_material_basis_in mutation in BGN on chromosome Xq28. | ||
| Also Known As | "MRLS" | ||
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| DO.org | |||
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monogenic disease |__X-linked monogenic disease__ disease | |__syndrome____________________| Meester-Loeys syndrome |
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X-linked monogenic disease syndrome |
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| MIM:300989 | |||