Genomics England

ataxin 7

Panel	Mode of inheritance	Details
Filter panels6 panels
Green in Adult onset hereditary spastic paraplegia R-numbers: R60 Signed-off version 5.5	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 7, OMIM:164500
Green in Adult onset neurodegenerative disorder R-numbers: R58 Signed-off version 7.10	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 7, OMIM:164500, autosomal dominant cerebellar ataxia type II, MONDO:0016163
Green in Ataxia and cerebellar anomalies - narrow panel Component of the following Super Panels: - Hereditary ataxia and cerebellar anomalies - childhood onset Signed-off version 7.19	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 7, OMIM:164500
Green in Hereditary ataxia with onset in adulthood R-numbers: R54 Signed-off version 7.11	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 7, OMIM:164500
Green in Hereditary neuropathy or pain disorder R-numbers: R78 Signed-off version 6.163	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 7, OMIM:164500
Green in Retinal disorders R-numbers: R32 Signed-off version 7.8	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 7, OMIM:164500, autosomal dominant cerebellar ataxia type II, MONDO:0016163