| Individual ID | 21933221.01 |
|---|---|
| Pubmed ID | 21933221 |
| Whose mosaic mutation | Father |
| Phenotypic Category | 1 |
| Age | 0.58 ~ 2.83 |
| Number of affected children | 2 ( male: 1; female: 1; ) |
| Disease | Isolated growth hormone deficiency type2(view all the variants in this disease) |
| OMIM ID | 173100 |