| Individual ID |
00234116 |
| Associated disease |
OI |
| Phenotype details |
blue sclerae (HP:000592); multiple fractures (HP:0002757) (20+); Forearm deformity; hearing loss (HP:0000365); dentinogenesis imperfecta (HP:0000703) |
| Diagnosis/Initial |
osteogenesis imperfecta |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
OI-1 |
| Age/Examination |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
Reduced type I procollagen |
| Owner name |
Global Variome, with Curator vacancy |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Global Variome, with Curator vacancy |
| Date created |
2019-01-13 12:23:00 +01:00 (CET) |
| Date last edited |
N/A |