377794 group of disorders
97935 Rare gastroenterologic disease
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117569 Rare intestinal disease
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104003 Congenital intestinal transport defect
104004 Intestinal disease due to vitamin absorption anomaly
104005 Intestinal disease due to fat malabsorption
104006 Congenital intestinal disease due to an enzymatic defect
104007 Congenital enteropathy involving intestinal mucosa development
104008 Short bowel syndrome
1
104009 Rare disease involving intestinal motility
104011 Rare tumor of intestine
5
104012 Rare inflammatory bowel disease
104013 Metabolic disease with intestinal involvement
2
36204 Intestinal lymphangiectasia
73014 Intractable diarrhea of infancy
94075 Severe immune-mediated enteropathy