congenital disorder of glycosylation type II SLC35A1-congenital disorder of glycosylation https://www.malacards.org/card/congenital_disorder_of_glycosylation_type_iif congenital disorder of glycosylation type 2f CDG-IIf Orphanet:238459 SLC35A1-CDG MEDGEN:370234 SLC35A1-CDG (CDG-IIf) congenital disorder of glycosylation, type IIf congenital disorder of glycosylation type IIf MESH:C567040 carbohydrate deficient glycoprotein syndrome type IIf SCTID:723624008 DOID:0070258 CDG2F SLC35A1-congenital disorder of glycosylation CDG syndrome type IIf 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. CMP-sialic acid transporter deficiency OMIM:603585 UMLS:C1970344 GARD:0012409 disorder of multiple glycosylation obsolete nephropathy secondary to a storage or other metabolic disease obsolete_SLC35A1-CDG