craniosynostosis, Herrmann-Opitz type
ORPHA: 2145
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 craniosynostosis, Herrmann-Opitz type, sourced from HPO and Orphanet clinical annotations.
Cleft palateBrachycephalyTurricephalyMalar flatteningHypertelorismMicrognathiaConvex nasal ridgeWebbed neckAbnormal rib morphologyAbnormality of the urethraBrachydactylySplit handCraniosynostosisIntrauterine growth retardationOligohydramniosMicromeliaShort noseShort statureFinger syndactylyAplasia/Hypoplasia of the lungsMicrotiaAbnormal antihelix morphologyAbnormality of the upper urinary tractCognitive impairment
Classification & Codes
Orphanet Code
ORPHA:2145craniosynostosis, Herrmann-Opitz type
| Orphanet | ORPHA:2145 |
| Treatments | 0 drug(s) |
| Symptoms on record | 24 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO