| Individual ID | 22987783.01 |
|---|---|
| Pubmed ID | 22987783 |
| Whose mosaic mutation | Mother |
| Phenotypic Category | 1 |
| Age | -1.0 ~ -1.0 |
| Number of affected children | 2 |
| Disease | Osteogenesis imperfecta type2(view all the variants in this disease) |
| OMIM ID | 166210 |
Found 3 variants in this database.