ALPI

alkaline phosphatase, intestinal
OMIM: 171740
PanelMode of inheritanceDetails
1 panel
R-numbers: R15
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Intestinal Alkaline Phosphatase deficiency, Inflammatory bowel disease, Autoinflammatory Disorders, ALPI deficiency