Genomics England
GMS Panels
Panels
Genes and Entities
ALPI
alkaline phosphatase, intestinal
OMIM:
171740
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Panel
Mode of inheritance
Details
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Primary immunodeficiency or monogenic inflammatory bowel disease
R-numbers:
R15
Signed-off version 6.12
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Intestinal Alkaline Phosphatase deficiency, Inflammatory bowel disease, Autoinflammatory Disorders, ALPI deficiency