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syndroom van keratoderma hereditarium mutilans met ichtyose (aandoening)
syndroom van keratoderma hereditarium mutilans met ichtyose
syndroom van keratodermie, ichtyosiforme dermatose en verhoogd bètaglucuronidase
ziekte van Camisa
Vohwinkel-syndroom met ichthyosis
syndroom van Vohwinkel met ichtyose
Keratoderma hereditarium mutilans with ichthyosis syndrome
Keratoderma ichthyosiform dermatosis elevated beta-glucuronidase syndrome
Camisa disease
Vohwinkel ichthyosis syndrome
A diffuse palmoplantar keratoderma with manifestation of honeycomb palmoplantar hyperkeratosis associated with pseudoainhum of the fifth digit of the hand, ichthyosis and deafness.Follows an autosomal dominant mode of transmission.
Id717183001
StatusPrimitive
Associated morphologyhyperkeratose
Finding sitegehele huid
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologyhyperkeratose
Finding sitestructuur van huid van voetzool
Has interpretationafwijkend
Interpretskeratinisatie
referentieset met complexe 'mapping' naar ICD-10
TargetQ82.8
RuleTRUE
AdviceALWAYS Q82.8
CorrelationSNOMED CT source code to target map code correlation not specified