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Hirschsprung disease

MONDO:0018309

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.

Also known as: HSCR, Hirschsprung disease, Hirschsprung disease susceptibility, Hirschsprung's disease, aganglionic megacolon, congenital intestinal aganglionosis, congenital megacolon, pelvirectal achalasia

31 clinical trials for this condition and its sub-types, 29 tagged with Hirschsprung disease itself.

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