genetische verstandelijke beperking	malformatiesyndroom met betrokkenheid van meerdere systemen	oculocutaan albinisme
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syndroom van gingivafibromatose, hypopigmentatie, microftalmie, oligofrenie en athetose (aandoening)
	syndroom van gingivafibromatose, hypopigmentatie, microftalmie, oligofrenie en athetose
	Cross syndrome
	Oculocerebral hypopigmentation syndrome Cross type Kramer syndrome Oculocerebral-hypopigmentation syndrome

Id	17827007
Status	Primitive

Associated morphology	verminderde melaninepigmentatie
Finding site	structuur van bulbus oculi
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	verminderde melaninepigmentatie
Finding site	structuur van huid
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Has interpretation	gestoord
Interprets	Adaptation behavior

Has interpretation	gestoord
Interprets	intellectueel vermogen

DHD Diagnosis thesaurus reference set

SNOMED CT to Orphanet simple map

2719

SNOMED CT to ICD-10 extended map

Target	E70.3
Rule	TRUE
Advice	ALWAYS E70.3 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified