Genomics England

ATXN10_ATTCT

ataxin 10

Panel	Mode of inheritance	Details
Filter panels6 panels
Green in Ataxia and cerebellar anomalies - childhood onset Component of the following Super Panels: - Hereditary ataxia and cerebellar anomalies, childhood onset Signed-off version 9.22	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 10, OMIM:603516, spinocerebellar ataxia type 10, MONDO:0011330
Green in Hereditary ataxia, adult onset Component of the following Super Panels: - Adult-onset neurological disorders Signed-off version 9.4	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 10, OMIM:603516
Green in Hereditary neuropathy or pain disorder R-numbers: R78 Signed-off version 8.30	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 10, OMIM:603516
Green in Hereditary spastic paraplegia, adult onset Component of the following Super Panels: - Adult-onset neurological disorders Signed-off version 6.13	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 10, OMIM:603516
Green in Hereditary spastic paraplegia, childhood onset R-numbers: R61 Signed-off version 9.7	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 10, OMIM:603516, spinocerebellar ataxia type 10, MONDO:0011330
Green in Neurodegenerative disorders, adult onset Component of the following Super Panels: - Adult-onset neurological disorders Signed-off version 9.4	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 10, OMIM:603516, spinocerebellar ataxia type 10, MONDO:0011330