Phenotype #0000242615
| Individual ID |
00322838 |
| 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 |
Raymond Dalgleish |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Raymond Dalgleish |
| Date created |
2008-08-01 16:29:11 +02:00 (CEST) |
| Date last edited |
2011-08-25 15:34:48 +02:00 (CEST) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|