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bn:24054338n
Noun Concept
NL
No term available
DE
Das Keratoderma hereditarium mutilans ist eine sehr seltene Genodermatose mit den Hauptmerkmalen massiver Hyperkeratose an den Hand- und Fußflächen, Mutilationen und Schwerhörigkeit bis Taubheit. Wikipedia
Relations
Sources
IS A
ziekte
genodermatose
zeldzame ziekte
syndroom
palmoplantaire keratoderma
HAS KIND
EN
Camisa disease
GENETIC ASSOCIATION
connexine-26-mutatie
HEALTH SPECIALTY
medische genetica
MODE OF INHERITANCE
EN
autosomal dominant

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