WDR26

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green WDR26 in Cerebral Palsy Level 2: Neurology and neurodevelopmental disorders Version 1.356	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Skraban-Deardorff syndrome MIM#617616
Green WDR26 in Mendeliome Version 1.1902	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Skraban-Deardorff syndrome, MIM#617616
Green WDR26 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.33 Component of the following Super Panels: Progressive Neurological Conditions	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Skraban-Deardorff syndrome MIM# 617616
Green WDR26 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genetic Health Queensland Phenotypes Skraban-Deardorff syndrome, MIM#617616
Amber WDR26 in Fetal anomalies Version 1.255	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Amber Genomics England PanelApp Phenotypes Skraban-Deardorff syndrome, MIM#617616 Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features

5 panels