Genomics England

myogenesis regulating glycosidase (putative)

Panel	Mode of inheritance	Details
Filter panels3 panels
Green in Adult onset dystonia, chorea or related movement disorder R-numbers: R56 Signed-off version 3.19	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Basal ganglia calcification, idiopathic, 7, autosomal recessive, OMIM:618317
Green in Adult onset neurodegenerative disorder R-numbers: R58 Signed-off version 5.4	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Basal ganglia calcification, idiopathic, 7, autosomal recessive, OMIM:618317
Green in White matter disorders and cerebral calcification - narrow panel Component of the following Super Panels: - Childhood onset leukodystrophy Signed-off version 4.3	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Basal ganglia calcification, idiopathic, 7, autosomal recessive, OMIM:618317