TNFAIP3

TNF alpha induced protein 3
OMIM: 191163
PanelMode of inheritanceDetails
1 panel
R-numbers: R15
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
A20 deficiency, Autoinflammatory syndrome, familial, Behcet-like, 616744, Autoimmune lymphoproliferative syndrome, Arthralgia, mucosal ulcers, ocular inflammation, Autoinflammatory Disorders