SLC35A1-congenital disorder of glycosylation

MONDO:0011342

SLC35A1-CDG is an extremely rare form of CDG syndrome characterized clinically in the single reported case by repeated hemorrhagic incidents, including severe pulmonary hemorrhage.

Also known as: CDG syndrome type IIf, CDG-IIf, CDG2F, CMP-sialic acid transporter deficiency, SLC35A1-CDG, SLC35A1-congenital disorder of glycosylation, carbohydrate deficient glycoprotein syndrome type IIf, congenital disorder of glycosylation type 2f

0 clinical trials for this condition and its sub-types, 0 tagged with SLC35A1-congenital disorder of glycosylation itself.

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↑ Disorder of multiple glycosylation (9) ↑ Congenital disorder of glycosylation type II (3)

Including sub-types (0) Tagged with SLC35A1-congenital disorder of glycosylation (0)

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