GRID2-related autosomal dominant spinocerebellar ataxia https://www.malacards.org/card/grid2_related_spinocerebellar_ataxia MONDO:0000563 the DO class DOID:0050988 is named 'GRID2-related spinocerebellar ataxia' and it is asserted to be AD. Most GRID18 mutations are AR, but it is rarelt AD [https://www.ncbi.nlm.nih.gov/books/NBK1138/; Coutelier et al [2015b]]. Here we assume the DO class refers to the rare AD form. Consider merging. DOID:0050988 GARD:0022804 autosomal dominant cerebellar ataxia