Goldenhar syndrome
MeSH: D006053ORPHA: 374
Overview
syndrome that is characterized by incomplete development of the ear, nose, soft palate, lip, and mandible. It is associated with anomalous development of the first branchial arch and second branchial arch
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
D006053Orphanet Code
ORPHA:374Goldenhar syndrome
| MeSH | D006053 |
| Orphanet | ORPHA:374 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO