Acanthosis nigricans	Autosomal recessive hereditary disorder	Developmental hereditary disorder	Ectodermal dysplasia	Inherited disorder of keratinization
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Ectodermal dysplasia with acanthosis nigricans syndrome (disorder)
	Lelis syndrome
	Ectodermal dysplasia with acanthosis nigricans syndrome
	The association of ectodermal dysplasia (hypotrichosis and hypohidrosis) with acanthosis nigricans. So far, only eight cases have been described in the literature. Other clinical features may include palmoplantar hyperkeratosis, nail dystrophy, intellectual deficit and hypodontia. Transmission is autosomal recessive.
	syndroom van ectodermale dysplasie met acanthosis nigricans
	Lelis-syndroom ectodermale dysplasie-acanthosis nigricans-syndroom syndroom van Lelis

Id	719429003
Status	Primitive

Associated morphology	Dysplasia
Finding site	Ectoderm structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Has interpretation	Abnormal
Interprets	Keratinization

Associated morphology	Morphologically abnormal structure
Finding site	Skin structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q82.4
Rule	TRUE
Advice	ALWAYS Q82.4 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

Target	L83
Rule	TRUE
Advice	ALWAYS L83
Correlation	SNOMED CT source code to target map code correlation not specified