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759.81 PRADER-WILLI SYNDROME


Code Information

Diagnosis Code: 759.81

Short Description: Prader-willi syndrome

Long Description: Prader-Willi syndrome

Code Classification:

  • Congenital anomalies (740–759)
    • Congenital anomalies (740-759)
      • 759 Other and unspecified congenital anomalies
        • 759.81 Prader-willi syndrome

Code Version: 2015 ICD-9-CM


References to Index of Diseases and Injuries

The code 759.81 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • Dystrophy, dystrophia 783.9
    • hypogenital, with diabetic tendency 759.81
  • Prader-Labhart-Willi-Fanconi syndrome (hypogenital dystrophy with diabetic tendency) 759.81
  • Prader-Willi syndrome (hypogenital dystrophy with diabetic tendency) 759.81
  • Syndrome - see also Disease
    • H3O 759.81
    • HHHO 759.81
    • hypotonia-hypomentia-hypogonadism-obesity 759.81
    • Prader (-Labhart)-Willi (-Fanconi) 759.81
    • Willi-Prader (hypogenital dystrophy with diabetic tendency) 759.81
  • Willi-Prader syndrome (hypogenital dystrophy with diabetic tendency) 759.81

Crosswalk Information

The code 759.81 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
759.81 Right Arrow Q87.1 Congenital malform syndromes predom assoc w short stature
This ICD-9 to ICD-10 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-9 Code ICD-9 Description
759.0 Anomalies of spleen
759.1 Anomalies of adrenal gland
759.2 Anomalies of other endocrine glands
759.3 Situs inversus
759.4 Conjoined twins
759.5 Tuberous sclerosis
759.6 Other hamartoses, not elsewhere classified
759.7 Multiple congenital anomalies, so described
759.82 Marfan syndrome
759.83 Fragile X syndrome
759.89 Other specified congenital anomalies
759.9 Congenital anomaly, unspecified

This page was last updated on: 10/1/2014

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