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Up to: Hereditary disease · Neurocristopathy · Intestinal motility disease

Hirschsprung disease

Hirschsprung disease (HSCR) is a congenital intestinal motility disorder that is characterized by signs of intestinal obstruction due to the presence of an aganglionic segment of variable extent in the terminal part of the colon.

29 trials tagged with this condition →

This condition has no sub-types.