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Hirschsprung disease

rare

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.

Identifiers
MONDO:0018309 Orphanet:388
Part of
Hereditary diseaseIntestinal motility diseaseNeurocristopathy
Also known as
aganglionic megacolon · congenital intestinal aganglionosis · congenital megacolon · Hirschsprung disease susceptibility · Hirschsprung's disease

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