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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
1 associated gene
6 signs/symptoms
APC-related attenuated familial adenomatous polyposis
Chronic intestinal pseudoobstruction

APC FLNA


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


APC-related attenuated familial adenomatous polyposis
APC
Chronic intestinal pseudoobstruction
FLNA



APC-related attenuated familial adenomatous polyposis
Chronic intestinal pseudoobstruction

Synonym(s):
- APC-related AFAP
- APC-related attenuated FAP
- APC-related attenuated familial polyposis coli

Synonym(s):
- CIPO

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

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

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

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


APC-related attenuated familial adenomatous polyposis

(no data available)