Keratoderma hereditarium mutilans

MONDO:0007422

Also known as: PPK mutilans and deafness, Vohwinkel syndrome, keratoderma hereditarium mutilans, mutilating keratoderma of Vohwinkel, mutilating keratoderma plus deafness, KHM, VOWNKL, deafness, congenital, with KERATOPACHYDERMIA and constrictions of fingers and toes

0 clinical trials for this condition and its sub-types, 0 tagged with Keratoderma hereditarium mutilans itself.

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↑ Hereditary disease (18235) ↑ Integumentary system disorder (4568)

Including sub-types (0) Tagged with Keratoderma hereditarium mutilans (0)

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