Orphanet: Central polydactyly
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Central polydactyly

Disease definition

A rare congenital limb malformation characterized by complete or partial duplication of one of the three middle digits in a hand or foot. It most commonly affects the fourth digit. The malformation may be unilateral or bilateral and can occur as an isolated defect or in association with other anomalies.

ORPHA:295004

Classification level: Disorder
  • Synonym(s):
    • Mesoaxial polydactyly
  • Prevalence: -
  • Inheritance: -
  • Age of onset: -
  • ICD-10: Q69.0
  • OMIM: -
  • UMLS: C0431903
  • MeSH: -
  • GARD: -
  • MedDRA: -

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The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.