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otospondylomegaepiphyseal dysplasia, autosomal dominant

ORPHA: 166100

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

human disease

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 otospondylomegaepiphyseal dysplasia, autosomal dominant, sourced from HPO and Orphanet clinical annotations.

GlossoptosisCleft palateMalar flatteningLong philtrumMicrognathiaSensorineural hearing impairmentPectus excavatumPectus carinatumOsteoarthritisArthralgiaAbnormal metacarpal morphologyExostoses

Classification & Codes

Orphanet Code

ORPHA:166100
otospondylomegaepiphyseal dysplasia, autosomal dominant
OrphanetORPHA:166100
Treatments0 drug(s)
Symptoms on record12 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO