Orphanet: Oculodentodigital dysplasia

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Oculodentodigital dysplasia

Disease definition

Oculodentodigital dysplasia (ODDD) is characterized by craniofacial, neurologic, limb and ocular abnormalities.


Classification level: Disorder
  • Synonym(s):
    • Meyer-Schwickerath syndrome
    • ODDD syndrome
    • Oculodentoosseous dysplasia
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant or Autosomal recessive 
  • Age of onset: Infancy, Neonatal
  • ICD-10: Q87.8
  • OMIM: 164200  257850
  • UMLS: C0812437
  • MeSH: -
  • GARD: 7239
  • MedDRA: 10063691
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