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Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder)
Keratoderma hereditarium mutilans with ichthyosis syndrome
Camisa disease
Vohwinkel ichthyosis syndrome
Keratoderma ichthyosiform dermatosis elevated beta-glucuronidase 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.
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
Id717183001
StatusPrimitive
Has interpretationAbnormal
InterpretsKeratinization
Associated morphologyHyperkeratosis
Finding siteEntire skin
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyHyperkeratosis
Finding siteSkin structure of sole of foot
Has interpretationImpaired
InterpretsHearing
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ82.8
RuleTRUE
AdviceALWAYS Q82.8
CorrelationSNOMED CT source code to target map code correlation not specified