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Vohwinkel syndrome [Supplementary Concept]

Deafness, congenital, with keratopachydermia and constrictions of fingers and toes

Date introduced: August 25, 2010

MeSH Unique ID: C536457

Heading Mapped to:

Entry Terms:

  • Mutilating keratoderma
  • Congenital Deafness with Keratopachydermia and Constrictions of Fingers and Toes
  • Palmoplantar Keratoderma Mutilans Vohwinkel
  • Ppk Mutilans Vohwinkel
  • Keratoderma hereditarium mutilans
  • Palmoplantar Keratoderma Mutilans

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