Albinism	Congenital deficiency of pigment of skin	Genetic disorder of skin pigmentation
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Phylloid hypomelanosis (disorder)
	Phylloid hypomelanosis
	bladvormige hypomelanose
	phylloïde hypomelanose

Id	403807001
Status	Primitive

Associated morphology	Decreased melanin pigmentation
Finding site	Skin structure
Occurrence	Congenital
Pathological process	Pathological developmental process

ICD-10 complex map reference set

Target	Q91.7
Rule	TRUE
Advice	ALWAYS Q91.7
Correlation	SNOMED CT source code to target map code correlation not specified