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Chronic intestinal pseudoobstruction

4 OMIM references -
1 associated gene
6 signs/symptoms

PROTEIN INTERACTIONS: 1

Fibronectin glomerulopathy

2 OMIM references -
1 associated gene
10 signs/symptoms

Chronic intestinal pseudoobstruction

Fibronectin glomerulopathy

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLNA	(0.72)	FN1

Citations in the biomedical literature:

Chronic intestinal pseudoobstruction		Fibronectin glomerulopathy
	Synonym(s): - CIPO		Synonym(s): - GFND - Glomerulopathy with fibronectin deposits

	Classification (Orphanet): (no data available)		Classification (Orphanet): - Rare genetic disease - Rare renal disease

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: 4 OMIM references - No MeSH references		External references: 2 OMIM references - No MeSH references

Chronic intestinal pseudoobstruction		Fibronectin glomerulopathy
	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		Very frequent - Autosomal dominant inheritance - Chronic arterial hypertension - Edema of the legs / lower limbs - Functional anomalies of the kidney and the urinary tract - Hematuria / microhematuria - Nephrotic syndrome - Proteinuria - Renal failure - Renal glomerular defect / glomerulopathy Occasional - Intracranial / cerebral / meningeal hemorrhage