LGI4

leucine rich repeat LGI family member 4
OMIM: 608303
PanelMode of inheritanceDetails
2 panels
R-numbers: R83
Signed-off version 4.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect, OMIM:617468
R-numbers: R21, R412
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ARTHROGRYPOSIS MULTIPLEX CONGENITA