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GENATLAS PHENOTYPE

last update : 18-06-2019

Symbol	MCPH23
Location	2q11.2
Name	microcephaly 23, primary, autosomal recessive
Corresponding gene	NCAPH
Main clinical features	primary microcephaly with a sloping forehead and moderate intellectual disability
Genetic determination	autosomal recessive
Function/system disorder	neurology
	osteo-articular
	mental retardation
Type	disease

Remark(s)