Up to now, the possible occurrence of a cationic ordering on the tetrahedral sublattices of stoichiometric double scheelite-type oxides was not settled, with somewhat contradictory X-ray diffraction and optical measurements [Blasse, G. J. Inorg. Nucl. Chem. 1968, 30, 2091]. Using two different synthesis routes, both ordered and disordered forms of fergusonite La2SiMoO8 were prepared. The crystal structure of the ordered form was determined using powder X-ray and neutron diffraction, which clearly evidence a tridimensional ordering between [SiO4] and [MoO4] tetrahedra. The crystal chemistry of ordered double sheelite-type La-2(III)((SiO4)-O-IV)-((MoO4)-O-VI) can be seen as an intermediate between those of simple regular scheelite or fergusonite Ln(III)((NbO4)-O-V) and of ordered triple scheelite Bi-3(III)((FeO4)-O-III)((MoO4)-O-VI)(2). The structure of the disordered La2SiMoO8 phase was analyzed using powder X-ray diffraction. A few small and larger diffraction peaks or bumps are observed in addition to the sharper peaks of a simple fergusonite cell. DIFFaX and FAULTS programs helped showing that these faint peaks originate from stacking faults between 2D ordered layers. The intermediate 2D-3D nature of SiO4/MoO4 ordering in seemingly disordered compounds might explain the previous discrepancy between optical and X-ray diffraction measurements.