Genomics England
GMS Panels
Panels
Genes and Entities

LGI3

leucine rich repeat LGI family member 3
OMIM: 608302
PanelMode of inheritanceDetails
3 panels
Green
in Arthrogryposis
R-numbers: R83
Signed-off version 10.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects, OMIM:620007
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects, OMIM:620007
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 10.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects, OMIM:620007