Intellectual disability	Multiple system malformation syndrome	Oculocutaneous albinism
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Cross syndrome (disorder)
	Cross syndrome
	Oculocerebral hypopigmentation syndrome Cross type Kramer syndrome Oculocerebral-hypopigmentation syndrome
	syndroom van gingivafibromatose, hypopigmentatie, microftalmie, oligofrenie en athetose

Id	17827007
Status	Primitive

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

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

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E70.3
Rule	TRUE
Advice	ALWAYS E70.3
Correlation	SNOMED CT source code to target map code correlation not specified