KCND2

potassium voltage-gated channel subfamily D member 2
OMIM: 605410, Gene2Phenotype

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Red KCND2 in Sudden death in young people Level 3: Cardiac arrhythmia Level 2: Cardiovascular disorders Version 1.16	review	Unknown	Sources Expert Review Red Other Radboud University Medical Center, Nijmegen Phenotypes J-wave syndrome with sudden cardiac death sudden arrhythmic death sudden cardiac arrest
Green KCND2 in DDG2P Version 6.424 Latest signed off version: v6.0 (30 Apr 2025) Component of the following Super Panels: Paediatric disorders	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources DD-Gene2Phenotype Expert Review Green Phenotypes KCND2-related neurodevelopmental disorder with or without seizures Tags de novo gene-checked
Green KCND2 in Early onset or syndromic epilepsy Level 2: Neurology Version 8.120 Latest signed off version: v8.0 (30 Apr 2025) Component of the following Super Panels: Paediatric disorders Unexplained death in infancy and sudden unexplained death in childhood	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Wessex and West Midlands GLH NHS GMS Expert Review Expert list Phenotypes epilepsy, NBO:0000642 seizure, HP:0001250 Tags gene-checked
Green KCND2 in Intellectual disability Level 2: Developmental disorders Version 9.279 Latest signed off version: v9.0 (30 Apr 2025) Component of the following Super Panels: Childhood onset leukodystrophy Hypotonic infant Paediatric disorders	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Literature Phenotypes global developmental delay, HP:0001263 Tags gene-checked