Phenotype #0000242623
| Individual ID |
00322867 |
| 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 |
Katarina Lindahl |
| Database submission license |
No license selected |
| Created by |
Katarina Lindahl |
| Date created |
2014-12-09 12:49:04 +01:00 (CET) |
| Date last edited |
2015-08-07 15:42:49 +02:00 (CEST) |
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