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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