Within the 400 CSF features, 18 analytes were specific to AD (such as GDA, PDE6D, FN1), seven to PD (SEMA4B, TNFSF8), and three to FTD (VSIG2, GLIPR1, IGFBP4), whereas 147 (AK2, EIF3G, MDH1) were shared by all diseases (Fig. 2C&E). This evidence concerns the gene PDE6D and Parkinson disease.