XX male syndrome
ICD-10: Q98.3MeSH: D058531ORPHA: 393
Overview
rare congenital condition where an individual with XX chromosomes is born with a penis and testes
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 XX male syndrome, sourced from HPO and Orphanet clinical annotations.
Male hypogonadismAmbiguous genitaliaPolycystic ovariesDecreased testicular size
Classification & Codes
ICD-10 Code
Q98.3MeSH Code
D058531Orphanet Code
ORPHA:393XX male syndrome
| ICD-10 | Q98.3 |
| MeSH | D058531 |
| Orphanet | ORPHA:393 |
| Treatments | 0 drug(s) |
| Symptoms on record | 4 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO