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Vohwinkel syndrome MeSH Supplementary Concept Data 2023


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 Number
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 Preferred
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