FASLG

PanelMode of inheritanceDetails
1 panel
R-numbers: R15
Signed-off version 6.0
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Phenotypes
Autoimmune lymphoproliferative syndrome, type IB, OMIM:601859, autoimmune lymphoproliferative syndrome type 1, MONDO:0011158, systemic lupus erythematosus (SLE)