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GENATLAS PHENOTYPE

last update : 15-12-2012

Symbol	SCKL6
Location	3q22
Name	Seckel syndrome 6
Corresponding gene	CEP63
Main clinical features	microcephaly, with head circumferences of -4 SD to -6 SD, speech delay and clear evidence of cognitive delay, proportionate short stature
Genetic determination	autosomal recessive
Function/system disorder	mental retardation
	neurology
Type	disease

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