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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 18/10/2005
Symbol CBG
Location 14q32.1
Name corticosteroid binding globulin deficiency
Corresponding gene SERPINA6
Main clinical features inflammatory disease
Genetic determination
Function/system disorder endocrinology
Type disease
Gene product
Name corticosteroid binding globulin (CBG)