Developmental hereditary disorder	Multiple malformation syndrome with facial defects as major feature	Trisomy Xq28	X-linked hereditary disease
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Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome (disorder)
	Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
	Methyl-CpG (cytosine phosphate guanine) binding protein-2 duplication syndrome Lubs X-linked intellectual disability syndrome Lubs X-linked mental retardation syndrome MECP2 duplication syndrome
	'methyl-cytosine phosphate guanine binding protein 2'-duplicatiesyndroom
	Lubs-Arena-syndroom syndroom van Lubs-Arena X-gebonden mentale retardatie Lubs type MECP2-duplicatiesyndroom

Id	702816000
Status	Primitive

Associated morphology	Morphologically abnormal structure
Finding site	Face structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Partial trisomy
Finding site	Sex chromosome X
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Partial trisomy
Finding site	Long arm of chromosome
Occurrence	Congenital
Pathological process	Pathological developmental process

ICD-10 complex map reference set

Target	Q99.8
Rule	TRUE
Advice	ALWAYS Q99.8
Correlation	SNOMED CT source code to target map code correlation not specified