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.

Synonyms: Congenital intestinal aganglionosis Aganglionic megacolon HSCR

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Term information

database cross reference
hasDbXref

OMIM:600155

MedDRA:10010539

ICD-10:Q43.1

OMIM:142623

OMIM:606874

OMIM:600156

OMIM:606875

MeSH:D006627

OMIM:613711

UMLS:C3661523

OMIM:613712

OMIM:611644

OMIM:608462

UMLS:C0019569

notation

ORPHA:388