Genomics England

phosphodiesterase 10A

Panel	Mode of inheritance	Details
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Green in Adult onset movement disorder R-numbers: R56 Signed-off version 2.1	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Striatal degeneration, autosomal dominant, OMIM:616922, Dyskinesia, limb and orofacial, infantile-onset, OMIM:616921
Green in Childhood onset dystonia or chorea or related movement disorder R-numbers: R57 Signed-off version 2.6	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Striatal degeneration, autosomal dominant 616922, Dyskinesia, limb and orofacial, infantile-onset 616921
Green in Paroxysmal central nervous system disorders R-numbers: R66 Signed-off version 2.1	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Dyskinesia, limb and orofacial, infantile-onset, 616921, Infantile-onset limb and orofacial dyskinesia