Autosomal dominant hereditary disorder	Congenital anomaly of foot	Congenital anomaly of hand	Congenital anomaly of skin	Congenital keratoderma	Congenital palmoplantar keratoderma	Developmental hereditary disorder	Hereditary diffuse palmoplantar keratoderma	Rough skin of hands
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Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder)
	Palmoplantar hyperkeratosis sclerodactyly syndrome
	Keratoderma with scleroatrophy of extremities Huriez syndrome Palmoplantar keratoderma sclerodactyly syndrome Scleroatrophic syndrome
	keratoderma palmoplantaris met sclero-atrofie
	syndroom van Huriez keratodermie met sclero-atrofie van extremiteit

Id	239076000
Status	Primitive

Associated morphology	Hyperkeratosis
Finding site	Entire skin of sole of foot
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Hyperkeratosis
Finding site	Entire skin of palmar area of hand
Occurrence	Congenital
Pathological process	Pathological developmental process

Has interpretation	Abnormal
Interprets	Keratinization

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q82.8
Rule	TRUE
Advice	ALWAYS Q82.8
Correlation	SNOMED CT source code to target map code correlation not specified