PTPN2

protein tyrosine phosphatase, non-receptor type 2
OMIM: 176887
PanelMode of inheritanceDetails
1 panel
R-numbers: R15
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Lupus, arthritis, common variable immunodeficiency, Very early onset inflammatory bowel disease