Q87.11 Prader-Willi syndrome
Billable / valid for submission ICD10CM Release FY2026
Version history
| Release | Valid from | Valid to | Description | Billable |
|---|---|---|---|---|
| FY2026 | 2025-10-01 | current | Prader-Willi syndrome | yes |
Related codes in Q87
- Q87 Other specified congenital malformation syndromes affecting multiple systems
- Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
- Q87.1 Congenital malformation syndromes predominantly associated with short stature
- Q87.19 Other congenital malformation syndromes predominantly associated with short stature
- Q87.2 Congenital malformation syndromes predominantly involving limbs
- Q87.3 Congenital malformation syndromes involving early overgrowth
- Q87.4 Marfan syndrome
- Q87.40 Marfan syndrome, unspecified
- Q87.41 Marfan syndrome with cardiovascular manifestations
- Q87.410 Marfan syndrome with aortic dilation
- Q87.418 Marfan syndrome with other cardiovascular manifestations
- Q87.42 Marfan syndrome with ocular manifestations
- Q87.43 Marfan syndrome with skeletal manifestation
- Q87.5 Other congenital malformation syndromes with other skeletal changes
- Q87.8 Other specified congenital malformation syndromes, not elsewhere classified
- Q87.81 Alport syndrome
- Q87.82 Arterial tortuosity syndrome
- Q87.83 Bardet-Biedl syndrome
- Q87.84 Laurence-Moon syndrome
- Q87.85 MED13L syndrome