Hirschsprung disease

Orpha code: 388OMIM code: 613712

Definition

A rare 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.

Disease data
Classification

Disease

Synonyms
Aganglionic megacolon
Aganglioza okrężnicy
HSCR
Wrodzona aganglionoza jelit
Colonic aganglionosis
Congenital intestinal aganglionosis
HSCR
ORPHA code
388
OMIM code
613712
ICD10 code
Q43.1
ICD11 code
LB16.1

No additional description.

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