Genomics England

prodynorphin

Panel	Mode of inheritance	Details
Filter panels2 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, imprinted status unknown	Phenotypes Spinocerebellar ataxia 23, OMIM:610245, spinocerebellar ataxia type 23, MONDO:0012449
Green in Hereditary neuropathy or pain disorder R-numbers: R78 Signed-off version 8.30	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Spinocerebellar ataxia 23, OMIM:610245, spinocerebellar ataxia type 23, MONDO:0012449