DOLK and DK1-congenital disorder of glycosylation: According to the Online Mendelian Inheritance in Man (OMIM) database, diseases associated with DOLK, DPM1, and DPM2 variants are designated as congenital disorders of glycosylation, type Im (CDG1M; 610768), type Ie (CDG1E; 608799), and type Iu (CDG1U) (615042), respectively.