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MIM:266265 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C
Echinobase Genes: slc35c1
Human Disease Resource: MIM
DOID:0050571 - congenital disorder of glycosylation type II |
DOID:6612 - leukocyte adhesion deficiency |
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DOID:0050571 - congenital disorder of glycosylation type II |
DOID:6612 - leukocyte adhesion deficiency |