Monarch Disease Ontology identifier MONDO_0011342 (SLC35A1-congenital disorder of glycosylation) can be described as follows. 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, carbohydrate deficient glycoprotein syndrome type IIf, congenital disorder of glycosylation type 2f, congenital disorder of glycosylation type IIf.