KDM3B

lysine demethylase 3B
OMIM: 609373
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Diets-Jongmans syndrome, OMIM:618846, Diets-Jongmans syndrome, MONDO:0030012