| Source | Code | Name | Case count | Share of cases (%) |
|---|---|---|---|---|
| OUTPAT | OUTPAT_ICD10(Q998) | Other specified chromosome abnormalities | 120 | |
| INPAT | INPAT_ICD10(Q998) | Other specified chromosome abnormalities | 41 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q998) | Other specified chromosome abnormalities. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 38 | |
| OUTPAT | OUTPAT_ICD10(Q992) | Fragile X chromosome | 29 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q992) | Fragile X chromosome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 16 | |
| INPAT | INPAT_ICD10(Q992) | Fragile X chromosome | 15 | |
| OUTPAT | OUTPAT_ICD10(Q999) | Chromosomal abnormality, unspecified | 9 | |
| INPAT | INPAT_ICD10(Q999) | Chromosomal abnormality, unspecified | 5 | |
| OUTPAT | OUTPAT_ICD10(Q990) | Chimera 46,XX/46,XY | 5 | |
| OUTPAT | OUTPAT_ICD10(Q991) | 46,XX true hermaphrodite | 5 |