LINGO1

leucine rich repeat and Ig domain containing 1
OMIM: 609791
PanelMode of inheritanceDetails
1 panel
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.79
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
LINGO1 related intellectual disability with microcephaly, speech and motor delay