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GENATLAS PHENOTYPE

last update : 19-10-2015

Symbol	MRD26
Location	7q11.22
Name	mental retardation, autosomal dominant 26
Corresponding gene	AUTS2
Main clinical features	intellectual disability, autism, short stature, microcephaly, cerebral palsy, and facial dysmorphisms, low birthweight, short stature, microcephaly, and feeding difficulties
Genetic determination	autosomal dominant
Function/system disorder	mental retardation
Type	disease

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