has material basis in germline mutation in CACNA1A spinocerebellar ataxia type 6 https://github.com/monarch-initiative/mondo/issues/5753 https://rarediseases.info.nih.gov/diseases/10351/spinocerebellar-ataxia-type-6 https://www.malacards.org/card/spinocerebellar_ataxia_6 DOID:0050956 MONDO:0008457 GARD:0010351 autosomal dominant cerebellar ataxia type III caused by mutation in CACNA1A UMLS:C0752124 MEDGEN:148458 NANDO:1200042 SCTID:715752006 icd11.foundation:1056119281 NCIT:C142838 OMIM:183086 Orphanet:98758 SCA6 spinocerebellar ataxia 6 CACNA1A autosomal dominant cerebellar ataxia type III Spinocerebellar ataxia type 6 (SCA6) is the most common subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by late-onset and slowly progressive gait ataxia and other cerebellar signs such as impaired muscle coordination and nystagmus. spinocerebellar ataxia type 6 autosomal dominant cerebellar ataxia type III CACNA1A-related complex neurodevelopmental disorder