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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
Gardner syndrome
Idiopathic bronchiectasis

APC CFTR
SCNN1A
SCNN1B
SCNN1G


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Gardner syndrome
APC
Idiopathic bronchiectasis
CFTR SCNN1A SCNN1B SCNN1G



Gardner syndrome
Idiopathic bronchiectasis

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare respiratory disease

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

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
1 MeSH reference: D005736
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.