Disease #05645 (AAT11 (aneurysm, aortic, thoracic, familial, type 11 (AAT11)), OMIM:617349)
| Official abbreviation |
AAT11 |
| Name |
aneurysm, aortic, thoracic, familial, type 11 (AAT11) |
| OMIM ID |
617349 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
FOXE3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
autosomal dominant |
| Date created |
2019-08-09 10:50:32 +02:00 (CEST) |
| Date last edited |
2025-11-10 16:34:30 +01:00 (CET) |
Individuals
|