has material basis in germline mutation in CWF19L1 syndromic intellectual disability autosomal recessive spinocerebellar ataxia 17 https://github.com/monarch-initiative/mondo/issues/5588 https://www.malacards.org/card/spinocerebellar_ataxia_autosomal_recessive_17 DOID:0080064 Any autosomal recessive congenital cerebellar ataxia in which the cause of the disease is a mutation in the CWF19L1 gene. Orphanet:453521 spinocerebellar ataxia autosomal recessive type 17 MEDGEN:863738 SCAR17 UMLS:C4015301 OMIM:616127 GARD:0017786 autosomal recessive cerebellar ataxia due to CWF19L1 deficiency spinocerebellar ataxia, autosomal recessive type 17 spinocerebellar ataxia, autosomal recessive 17 MONDO:0014503 autosomal recessive spinocerebellar ataxia type 17 CWF19L1 autosomal recessive congenital cerebellar ataxia autosomal recessive congenital cerebellar ataxia caused by mutation in CWF19L1 autosomal recessive congenital cerebellar ataxia