| Individual ID | 2339700.01 |
|---|---|
| Pubmed ID | 2339700 |
| Whose mosaic mutation | Father |
| Phenotypic Category | 1 |
| Number of affected children | 1 ( male: 1; ) |
| Disease | Osteogenesis imperfecta type2(view all the variants in this disease) |
| OMIM ID | 166210 |
Found 2 variants in this database.