Furthermore, we visually inspected automatically generated segmentations of several clinically diagnosed sporadic and hereditary ataxias to verify whether CerebNet generalizes to other pathologies (N=14: two randomly selected cases of MSA-C, RFC1, SCA1, SCA2 and SCA6, AOA2 as well as one case of SYNE1 and CTX each, including cases with severe atrophy, see also Fig. 9 in the Appendix). This evidence concerns the gene CACNA1A and multiple system atrophy, cerebellar type.