Phenotype #0000310071
| Individual ID |
00418775 |
| Associated disease |
SGS |
| Phenotype details |
mitral valve prolapse, aneurismatic ovale fossa, megalocornea, joint hypermobility, Intellectual disability |
| Diagnosis/Initial |
Aortic valvular disease |
| Inheritance |
Familial |
| Diagnosis/Definite |
Shprintzen–Goldberg Syndrome |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Carmela Fusco |
| Database submission license |
No license selected |
| Created by |
Carmela Fusco |
| Date created |
2022-10-06 13:44:12 +02:00 (CEST) |
| Date last edited |
2022-10-07 10:42:40 +02:00 (CEST) |
|