Phenotype #0000323045
| Individual ID |
00432483 |
| Associated disease |
OI1 |
| Phenotype details |
- |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
- |
| Age/Examination |
10y (10 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Kim Worring |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Kim Worring |
| Date created |
2023-02-23 11:36:18 +01:00 (CET) |
| Date last edited |
2023-02-23 13:46:54 +01:00 (CET) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|