PRDM8

PR/SET domain 8
OMIM: 616639, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Red PRDM8 in Early onset or syndromic epilepsy Level 3: Inherited Epilepsy Syndromes Level 2: Neurology and neurodevelopmental disorders Version 4.193 Latest signed off version: v4.0 (22 Mar 2023) Component of the following Super Panels: Unexplained death in infancy and sudden unexplained death in childhood	review	BIALLELIC, autosomal or pseudoautosomal	Sources NHS GMS Expert Review Red Wessex and West Midlands GLH Phenotypes ?Epilepsy, progressive myoclonic, 10, 616640

Panel

Reviews

Mode of inheritance

Details

Red PRDM8 in Early onset or syndromic epilepsy

Level 3: Inherited Epilepsy Syndromes
Level 2: Neurology and neurodevelopmental disorders
Version 4.193
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

Unexplained death in infancy and sudden unexplained death in childhood

review

BIALLELIC, autosomal or pseudoautosomal

Sources

NHS GMS
Expert Review Red
Wessex and West Midlands GLH

Phenotypes

?Epilepsy, progressive myoclonic, 10, 616640