Q87.11 Prader-Willi syndromeBillable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis. Exempt from present-on-admission (POA) reporting.
Defines the logic of DRG(s) 564-566 in MDC 08.
E23.3 Hypothalamic dysfunction, not elsewhere classified ("Prader-Willi syndrome (Q87.11)")E66 Overweight and obesity ("Prader-Willi syndrome (Q87.11)")Q67 Congenital musculoskeletal deformities of head, face, spine and chest ("congenital malformation syndromes classified to Q87.-")Q75 Other congenital malformations of skull and face bones ("congenital malformation syndromes classified to Q87.-")Q89.7 Multiple congenital malformations, not elsewhere classified ("congenital malformation syndromes affecting multiple systems (Q87.-)")Q87 Other specified congenital malformation syndromes affecting multiple systemsQ87.0 Congenital malformation syndromes predominantly affecting facial appearanceQ87.1 Congenital malformation syndromes predominantly associated with short statureQ87.11 Prader-Willi syndrome (this code)Q87.19 Other congenital malformation syndromes predominantly associated with short statureQ87.2 Congenital malformation syndromes predominantly involving limbsQ87.3 Congenital malformation syndromes involving early overgrowthQ87.4 Marfan syndromeQ87.40 Marfan syndrome, unspecified