ODCs

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1 OMIM reference -
1 associated gene
5 signs/symptoms

COMMON GENES: 1

2 OMIM references -
4 associated genes
No signs/symptoms info

Multiple intestinal atresia

Autosomal recessive early-onset inflammatory bowel disease

Citations in the biomedical literature:

Multiple intestinal atresia		Autosomal recessive early-onset inflammatory bowel disease
	Synonym(s): - Familial intestinal polyatresia syndrome		Synonym(s): - Autosomal recessive early-onset IBD

	Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare genetic disease		Classification (Orphanet): - Rare gastroenterologic disease - Rare genetic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the digestive system -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - No MeSH references

Multiple intestinal atresia
	Very frequent - Autosomal recessive inheritance - Duodenal atresia / stenosis / megaduodenum - Intestinal atresia / stenosis / absence / agenesis / hypoplasia (excludes duodenum) - Stillbirth / neonatal death Frequent - Polyhydramnios
Autosomal recessive early-onset inflammatory bowel disease
(no data available)