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2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Congential Anomalies 740-759 > Other Congenital Anomalies Of Digestive System 751.* >

2008 ICD-9-CM Diagnosis 751.3

Hirschsprung's disease and other congenital functional disorders of colon

  • Congenital MEGACOLON resulting from the absence of ganglion cells (aganglionosis) in a distal segment of the LARGE INTESTINE. The aganglionic segment is permanently contracted thus causing dilatation proximal to it. In most cases, the aganglionic segment is within the RECTUM and SIGMOID COLON.
  • 751.3 is a specific code that can be used to specify a diagnosis
  • 751.3 contains 22 index entries
  • View the ICD-9-CM Volume 1 751.* hierarchy

751.3 also known as:

  • Aganglionosis
  • Congenital dilation of colon
  • Congenital megacolon
  • Marcrocolon


Index entries containing 751.3:

Achalasia 530.0
  • pelvirectal 751.3
Aganglionosis (bowel) (colon) 751.3
Dilatation
  • colon 564.7
    • congenital 751.3
Disease, diseased - see also Syndrome
  • colon 569.9
    • functional 564.9
      • congenital 751.3
  • Hirschsprung's (congenital megacolon) 751.3
  • intestine 569.9
    • functional 564.9
      • congenital 751.3
  • Myà's (congenital dilation, colon) 751.3
  • Ruysch's (Hirschsprung's disease) 751.3
Disorder - see also DiseaseExcess, excessive, excessively
  • large
    • colon 564.7
      • congenital 751.3
Giant
  • colon (congenital) 751.3
Hirschsprung's disease or megacolon (congenital) 751.3
Hypertrophy, hypertrophicMacrocolon (congenital) 751.3
Macrosigmoid 564.7
  • congenital 751.3
Megacolon (acquired) (functional) (not Hirschsprung's disease) 564.7
  • aganglionic 751.3
  • congenital, congenitum 751.3
  • Hirschsprung's (disease) 751.3
Megasigmoid 564.7
  • congenital 751.3
Myà's disease (congenital dilation, colon) 751.3
Ruysch's disease (Hirschsprung's disease) 751.3