104003 Congenital intestinal transport defect

104004 Intestinal disease due to vitamin absorption anomaly

104006 Congenital intestinal disease due to an enzymatic defect

104007 Congenital enteropathy involving intestinal mucosa development

104009 Rare disease involving intestinal motility

104013 Metabolic disease with intestinal involvement 2

363300 Genetic intractable diarrhea of infancy

363306 Genetic intestinal disease due to fat malabsorption

363314 Genetic intestinal polyposis

365563 Primary short bowel syndrome