WAGR syndrome
MeSH: D017624ORPHA: 893
Overview
rare genetic syndrome in which affected children are predisposed to develop Wilms tumour
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with WAGR syndrome, sourced from HPO and Orphanet clinical annotations.
CryptorchidismAmbiguous genitaliaEverted lower lip vermilionMicrocephalyMicrognathiaHearing abnormalityGlaucomaVisual impairmentPtosisCataractNystagmusIntellectual disabilityObesityScoliosisShort statureDysfunction of lateral corticospinal tractsAplasia/Hypoplasia of the irisDisplacement of the urethral meatus
Classification & Codes
MeSH Code
D017624Orphanet Code
ORPHA:893WAGR syndrome
| MeSH | D017624 |
| Orphanet | ORPHA:893 |
| Treatments | 0 drug(s) |
| Symptoms on record | 18 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO