Phenotype #0000242621
| Individual ID |
00322865 |
| Associated disease |
EDS |
| Inheritance |
- |
| Diagnosis/Initial |
- |
| Age/Examination |
- |
| Diagnosis/Definite |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Phenotype details |
Osteogenesis imperfecta/Ehlers-Danlos syndrome overlap, |
| Hearing/Loss |
- |
| Protein |
- |
| CK-level |
- |
| EMG |
- |
| Muscle/Biopsy |
- |
| Age/Diagnosis |
- |
| Owner name |
Sofie Symoens |
| Database submission license |
No license selected |
| Created by |
Sofie Symoens |
| Date created |
2011-09-27 13:13:27 +02:00 (CEST) |
| Date last edited |
2013-05-23 13:07:43 +02:00 (CEST) |
|