MeSH Browser

MeSH Supplementary: Vohwinkel syndrome
Unique ID: C536457
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536457
Entry Term(s): Congenital Deafness with Keratopachydermia and Constrictions of Fingers and Toes; Keratoderma hereditarium mutilans; Mutilating keratoderma; Palmoplantar Keratoderma Mutilans; Palmoplantar Keratoderma Mutilans Vohwinkel; Ppk Mutilans Vohwinkel
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple; *Hand Deformities, Congenital; *Hearing Loss, Sensorineural; *Keratoderma, Palmoplantar
Frequency: 15
Note: Deafness, congenital, with keratopachydermia and constrictions of fingers and toes
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Vohwinkel syndrome MeSH Supplementary Concept Data 2025