759.81 - Prader-Willi Syndrome
The ICD 9 Code for Prader-Willi syndrome is listed as 759.81.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.
| ICD 9 CM Field | Value |
|---|---|
| Diagnosis Code: | 759.81 |
| Long Description: | Prader-Willi syndrome |
| Short Description: | Prader-willi syndrome |
| Chapter: | Congenital Anomalies |
| Block: | Other and unspecified congenital anomalies (759-759) |
| ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD-10-CM Code: | Q87.1 - Congenital malformation syndromes predominantly associated with short stature (approximate) |
| ICD-9-CM Siblings (same level / similar specificity) of 759.81: | |
| 759.82 - Marfan syndrome | |
| 759.83 - Fragile X syndrome | |
| 759.89 - Other specified congenital anomalies | |