PDE10A

phosphodiesterase 10A
OMIM: 610652, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Red PDE10A in Cerebral Palsy Level 2: Neurology and neurodevelopmental disorders Version 1.389	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Dyskinesia, limb and orofacial, infantile-onset, autosomal recessive, MIM#616921 Striatal degeneration, autosomal dominant, MIM#616922
Green PDE10A in Mendeliome Version 1.2302	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Dyskinesia, limb and orofacial, infantile-onset, MIM#616921 Striatal degeneration, autosomal dominant, MIM# 616922
Green PDE10A in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genetic Health Queensland Phenotypes Dyskinesia, limb and orofacial, infantile-onset, MIM#616921
Green PDE10A in Dystonia - isolated/combined Level 2: Neurology and neurodevelopmental disorders Version 1.37 Component of the following Super Panels: Dystonia_Superpanel Progressive Neurological Conditions Tremors_Superpanel	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Early onset chorea without epilepsy infantile onset limb and orofacial dyskinesia (OMIM 616921)
Red PDE10A in Fetal anomalies Version 1.313	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red Genomics England PanelApp Genetic Health Queensland Phenotypes Dyskinesia, limb and orofacial, infantile-onset, MIM#616921 Striatal degeneration, autosomal dominant, MIM#616922