Developmental hereditary disorder	Multiple system malformation syndrome	X-linked dominant hereditary disease
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Oculofaciocardiodental syndrome (disorder)
	Oculofaciocardiodental syndrome
	Microphthalmia, cataract, radiculomegaly and septal heart defect Oculo-facio-cardio-dental syndrome Microphthalmia syndromic 2
	oculofaciocardiodentaal syndroom
	microftalmie-cataract-radiculomegalie-hartseptumdefect-syndroom MCOPS2 syndromale microftalmie 2 OFCD-syndroom syndroom met microftalmie, cataract, radiculomegalie en hartseptumdefect

Id	699300009
Status	Primitive

Associated morphology	Morphologically abnormal structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8
Correlation	SNOMED CT source code to target map code correlation not specified