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Chronic intestinal pseudoobstruction

4 OMIM references -
1 associated gene
6 signs/symptoms

PROTEIN INTERACTIONS: 1

Atypical Werner syndrome

1 associated gene
No signs/symptoms info

Chronic intestinal pseudoobstruction

Atypical Werner syndrome

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLNA	(0.73)	LMNA

Citations in the biomedical literature:

Chronic intestinal pseudoobstruction		Atypical Werner syndrome
	Synonym(s): - CIPO		Synonym(s): - Atypical progeroid syndrome

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

	Classification (ICD10): - Diseases of the digestive system -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	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
Atypical Werner syndrome
(no data available)