GPHN and even-plus syndrome: For example, MAN2C1 is associated with congenital disorder of deglycosylation 2 (MIM #619775), GPHN with molybdenum cofactor deficiency C (MIM #615501), LRP2 with Donnai–Barrow syndrome (MIM #222448), and HSPA9 with Even-plus syndrome (MIM #616854).