Autosomal dominant hereditary disorder	Congenital anomaly of skin	Developmental hereditary disorder	Hereditary disorder of the integument	Lentiginosis
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Multiple lentigines syndrome (disorder)
	Multiple lentigines syndrome
	Leopard syndrome Leopard syndrome lentiginosis LEOPARD syndrome
	LEOPARD-syndroom
	lentiginosis profusa

Id	111306001
Status	Primitive

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

Associated morphology	Lentigo
Finding site	Structure of skin and/or mucous membrane

PALGA thesaurus simple reference set for pathology

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	L81.4
Rule	TRUE
Advice	ALWAYS L81.4
Correlation	SNOMED CT source code to target map code correlation not specified