Vohwinkel syndrome (Q7939442)
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human disease
- PPK mutilans and deafness
- keratoderma hereditarium mutilans
- Mutilating Keratoderma
- Mutilating keratoderma of Vohwinkel
- DEAFNESS, CONGENITAL, WITH KERATOPACHYDERMIA AND CONSTRICTIONS OF FINGERS AND TOES
- Mutilating keratoderma plus deafness
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Vohwinkel syndrome |
human disease |
|
Statements
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757.39
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Identifiers
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Sitelinks
Wikipedia(2 entries)
- dewiki Keratoderma hereditarium mutilans
- enwiki Vohwinkel syndrome