fibular dimelia-diplopodia syndrome

ORPHA: 1757

Overview

Fibular dimelia-diplopodia syndrome is a rare developmental anomaly

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 fibular dimelia-diplopodia syndrome, sourced from HPO and Orphanet clinical annotations.

Absent tibiaAbnormality of the faceSacrococcygeal teratoma

Classification & Codes

Orphanet Code

ORPHA:1757
fibular dimelia-diplopodia syndrome
OrphanetORPHA:1757
Treatments0 drug(s)
Symptoms on record3 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO