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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
4 associated genes
No signs/symptoms info
Intestinal epithelial dysplasia
Idiopathic bronchiectasis

EPCAM CFTR
SCNN1A
SCNN1B
SCNN1G


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
EPCAM
(0.72)
CFTR



Citations in the biomedical literature:


Intestinal epithelial dysplasia
EPCAM
Idiopathic bronchiectasis
CFTR SCNN1A SCNN1B SCNN1G



Intestinal epithelial dysplasia
Idiopathic bronchiectasis

Synonym(s):
- Congenital familial intractable diarrhea with epithelial or epithelium abnormalities
- IED
- Tufting enteropathy

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
Classification (Orphanet):
- Rare respiratory disease

Classification (ICD10):
- Certain conditions originating in the perinatal period -
Classification (ICD10):
- Diseases of the respiratory system -

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

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

No signs/symptoms info available.