CODAS syndrome

MeSH: C536434ORPHA: 1458

Overview

Codas syndrome is a multiple congenital anomalies syndrome characterized by Cerebral, Ocular, Dental, Auricular and Skeletal anomalies

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 CODAS syndrome, sourced from HPO and Orphanet clinical annotations.

EpicanthusOverfolded helixAnteverted naresCataractAbnormal dental enamel morphologyDelayed eruption of teethBrachydactylyGlobal developmental delayDelayed skeletal maturationShort noseAbnormal form of the vertebral bodiesCoronal cleft vertebraeMidline defect of the noseShort statureDepressed nasal bridgeAbnormal epiphysis morphologyAbnormal dental morphologyCrumpled earShort metacarpalFlat faceSensorineural hearing impairmentPtosisHypotoniaCongenital hip dislocationAbnormal pelvic girdle bone morphologyScoliosisHydroureterStrabismusNystagmusAbnormality of the larynxVentricular septal defectExtrahepatic biliary duct atresiaJoint hypermobility

Classification & Codes

MeSH Code

C536434

Orphanet Code

ORPHA:1458
CODAS syndrome
MeSHC536434
OrphanetORPHA:1458
Treatments0 drug(s)
Symptoms on record33 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
CODAS syndrome | OrphanDrug