Autosomal recessive hereditary disorder
Hereditary diffuse palmoplantar keratoderma
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Hereditary palmoplantar keratoderma Gamborg Nielsen type (disorder)
Hereditary palmoplantar keratoderma Gamborg Nielsen type
The presence of diffuse palmoplantar keratoderma without associated symptoms. The syndrome has been described in multiple families from the northernmost county of Sweden (Norrbotten). The palmoplantar keratoderma found in the Gamborg-Nielsen type disease is milder than that found in Mal de Meleda but more severe than that found in Thost-Unna palmoplantar keratoderma. Transmission is autosomal recessive.
hereditaire palmoplantaire keratodermie Gamborg-Nielsen-type
erfelijke keratosis palmoplantaris type Gamborg-Nielsen
Id717228004
StatusPrimitive
Associated morphologyHyperkeratosis
Finding siteEntire skin of sole of foot
Associated morphologyHyperkeratosis
Finding siteEntire skin of palmar area of hand
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