has material basis in germline mutation in TTBK2 spinocerebellar ataxia type 11 https://www.malacards.org/card/spinocerebellar_ataxia_11 GARD:0010475 icd11.foundation:743674840 spinocerebellar ataxia 11 spinocerebellar ataxia type 11 Spinocerebellar ataxia type 11 (SCA11) is a subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by the early-onset of cerebellar signs, eye movement abnormalities and pyramidal signs. SCTID:719207000 SCA11 Orphanet:98767 MESH:C565772 DOID:0050961 OMIM:604432 MEDGEN:346799 UMLS:C1858351 MONDO:0011464 autosomal dominant cerebellar ataxia type III