Any autosomal recessive congenital cerebellar ataxia in which the cause of the disease is a mutation in the CWF19L1 gene.
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autosomal recessive spinocerebellar ataxia 2
MONDO:0008943
cerebellar ataxia, intellectual disability, and dysequilibrium
MONDO:0009133
Cayman type cerebellar ataxia
MONDO:0011025
Joubert syndrome and related disorders
MONDO:0015369
CAMOS syndrome
MONDO:0019374
congenital cerebellar ataxia due to RNU12 mutation
MONDO:0033717