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Prader-Willi Syndrome

ICD-10: LD90.3MeSH: D011218ORPHA: ORPHA:7391 Treatment Available

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

A rare genetic imprinting disorder caused by loss of paternally expressed genes on chromosome 15q11-q13. Characterized by neonatal hypotonia, hyperphagia with risk of severe obesity, short stature, and intellectual disability.

Available Treatments (1)

DrugFormStatusCountriesLead Time
diazoxide choline
Orphan
—FDA Approved (2025)1—

Classification & Codes

ICD-10 Code

LD90.3

MeSH Code

D011218

Orphanet Code

ORPHA:ORPHA:739
Prader-Willi Syndrome
ICD-10LD90.3
MeSHD011218
OrphanetORPHA:ORPHA:739
Treatments1 drug(s)
Statuspublished

Treatment Summary

diazoxide choline· Orphan
Factual Authority
Last Updated7/24/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO