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GENATLAS PHENOTYPE

last update : 20-12-2021

Symbol	AGM9
Location	6p32.1
Name	agammaglobulinemia 9, autosomal recessive
Corresponding gene	SLC39A7
Main clinical features	primary immunodeficiency characterized by recurrent bacterial infections associated with agammaglobulinemia and absence of circulating B cells additional features include failure to thrive and skin involvement
Genetic determination	autosomal recessive
Function/system disorder	defense and immunity
Type	disease

Remark(s)