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Diseases

Genetic and Rare Diseases Information Center (GARD)

Vohwinkel syndrome


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Other Names for Vohwinkel syndrome

  • Deafness, congenital, with keratopachydermia and constrictions of fingers and toes
  • Keratoderma hereditarium mutilans
  • KHM
  • Mutilating keratoderma
  • Mutilating keratoderma of Vohwinkel
  • Mutilating keratoderma plus deafness
  • PPK mutilans and deafness
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.