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Chronic intestinal pseudoobstruction

4 OMIM references -
1 associated gene
6 signs/symptoms

PROTEIN INTERACTIONS: 1

Atelosteogenesis type III

1 OMIM reference -
1 associated gene
No signs/symptoms info

Chronic intestinal pseudoobstruction

Atelosteogenesis type III

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLNA	(0.95)	FLNB

Citations in the biomedical literature:

Chronic intestinal pseudoobstruction		Atelosteogenesis type III
	Synonym(s): - CIPO		Synonym(s): - AO3 - AOIII

	Classification (Orphanet): (no data available)		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare maxillo-facial surgical disease - Rare neurologic disease - Rare otorhinolaryngologic disease

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal dominant

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - 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
Atelosteogenesis type III
(no data available)