Disease #00027 (OI (Osteogenesis imperfecta))
Official abbreviation |
OI |
Name |
Osteogenesis imperfecta |
OMIM ID |
- |
Inheritance |
- |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 2 genes |
COL1A1, COL1A2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|