Autosomal dominant hereditary disorder	Café au lait spots	Congenital disease	Genetic disorder of skin pigmentation	Hyperpigmentation of skin
\|	\|	\|	\|	\|

Neurofibromatosis type 1-like syndrome (disorder)
	Legius syndrome
	NFLS - neurofibromatosis type 1-like syndrome Neurofibromatosis type 1-like syndrome
	'neurofibromatosis-1-like'-syndroom
	Legius-syndroom syndroom van Legius

Id	703541007
Status	Primitive

Associated morphology	Hyperpigmentation
Finding site	Skin structure
Occurrence	Congenital

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q85.8
Rule	TRUE
Advice	ALWAYS Q85.8
Correlation	SNOMED CT source code to target map code correlation not specified