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Results 1 - 10 of 15 for "Hirschsprung's" disease
  1. Hirschsprung disease 
    ... disease. Aganglionic megacolon Congenital intestinal aganglionosis Congenital megacolon Hirschsprung's disease HSCR Genetic Testing Registry: Hirschsprung disease, susceptibility to, ...
    https://medlineplus.gov/genetics/condition/hirschsprung-disease - Genetics
  2. EDN3 gene 
    ... relationship between EDN-3 gene, EDNRB gene and Hirschsprung's disease. World J Gastroenterol. 2003 Dec;9(12):2839- ... the endothelin-3 (EDN-3) gene in isolated Hirschsprung's disease. Pediatr Res. 1999 May;45(5 Pt 1): ...
    https://medlineplus.gov/genetics/gene/edn3 - Genetics
  3. Mowat-Wilson syndrome 
    ... intellectual disability, delayed development, an intestinal disorder called Hirschsprung disease, and other birth defects.Children with Mowat-Wilson ... syndrome are born with an intestinal disorder called Hirschsprung disease that causes severe constipation, intestinal blockage, and enlargement ...
    https://medlineplus.gov/genetics/condition/mowat-wilson-syndrome - Genetics
  4. RET gene 
    ... RET gene is a major risk factor for Hirschsprung's disease: a meta-analysis. Pediatr Surg Int. 2015 Aug; ...
    https://medlineplus.gov/genetics/gene/ret - Genetics
  5. EDNRB gene 
    ... relationship between EDN-3 gene, EDNRB gene and Hirschsprung's disease. World J Gastroenterol. 2003 Dec;9(12):2839- ...
    https://medlineplus.gov/genetics/gene/ednrb - Genetics
  6. Congenital central hypoventilation syndrome 
    ... in the nerves that control the digestive tract (Hirschsprung disease), resulting in severe constipation, intestinal blockage, and enlargement ... researchers refer to the combination of CCHS and Hirschsprung disease as Haddad syndrome.) Some affected individuals develop learning ...
    https://medlineplus.gov/...ngenital-central-hypoventilation-syndrome - Genetics
  7. Emanuel syndrome 
    ... the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's disease. J Pediatr Surg. 2007 Nov;42(11):1928- ...
    https://medlineplus.gov/genetics/condition/emanuel-syndrome - Genetics
  8. Bardet-Biedl syndrome 
    Bardet-Biedl syndrome is a disorder that affects many parts of the body. The signs and symptoms of this condition vary among affected individuals, even among ...
    https://medlineplus.gov/genetics/condition/bardet-biedl-syndrome - Genetics
  9. SOX10 gene 
    ... II and type IV (also known as Waardenburg-Hirschsprung disease or Waardenburg-Shah syndrome). Both types of Waardenburg ... type IV also have an intestinal disorder called Hirschsprung disease that causes severe constipation or intestinal blockage. Most ...
    https://medlineplus.gov/genetics/gene/sox10 - Genetics
  10. L1CAM gene 
    ... buildup of fluid in the brain (hydrocephalus) and Hirschsprung disease. Hirschsprung disease is an intestinal disorder characterized by the absence ... the brain and intestine, leading to hydrocephalus and Hirschsprung disease. antigen identified by monoclonal antibody R1 CAML1 CD171 ...
    https://medlineplus.gov/genetics/gene/l1cam - Genetics
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