Vohwinkel-Syndrom (klassische Form)
DEAFNESS, CONGENITAL, WITH KERATOPACHYDERMIA AND CONSTRICTIONS OF FINGERS AND TOES
OMIM: 124500
Synonyme
- Keratoderma hereditarium mutilans
- KHM
- VOHWINKEL SYNDROME
- MUTILATING KERATODERMA
- KERATODERMA HEREDITARIUM MUTILANS; KHM
Gen locations
- GJB2(OMIM 121011)