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GENATLAS PHENOTYPE

last update : 17-01-2015

Symbol	MRX80
Location	Xq23
HGNC id	18872
Name	mental retardation, 80
Corresponding gene	ALG13
Main clinical features	non specific form of X-linked mental retardation intellectual disability is the sole clinically consistent manifestation
Genetic determination	sex linked
Function/system disorder	mental retardation
Type	disease

Remark(s)

in the same interval than MRX35, and MRX23, MRX27