KIRREL3

kirre like nephrin family adhesion molecule 3
OMIM: 607761
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 8.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Intellectual developmental disorder, autosomal dominant 4, OMIM:612581, intellectual disability, autosomal dominant 4, MONDO:0012947