ODCs

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4 OMIM references -
1 associated gene
6 signs/symptoms

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Chronic intestinal pseudoobstruction

Familial adenomatous polyposis due to 5q22.2 microdeletion


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLNA	(0.63)	APC

Citations in the biomedical literature:

Chronic intestinal pseudoobstruction		Familial adenomatous polyposis due to 5q22.2 microdeletion
	Synonym(s): - CIPO		Synonym(s): - Colorectal adenomatous polyposis due to monosomy 5q22.2 - FAP due to monosomy 5q22.2 - Familial adenomatous polyposis due to del(5)(q22.2) - Familial adenomatous polyposis due to monosomy 5q22.2 - Familial polyposis coli due to monosomy 5q22.2

	Classification (Orphanet): (no data available)		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease

	Classification (ICD10): - Diseases of the digestive system -		Classification (ICD10): - Neoplasms -

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

	External references: 4 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

Chronic intestinal pseudoobstruction
	Very frequent - Intestinal / colonic anomaly Frequent - Gastric / pyloric stenosis - Intestinal / gut / bowel malrotation - Structural anomalies of the nervous system Occasional - Patent ductus arteriosus - Platelets shape anomalies
Familial adenomatous polyposis due to 5q22.2 microdeletion
(no data available)