Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
4 associated genes
No signs/symptoms info
CLN11 disease
Idiopathic bronchiectasis

GRN CFTR
SCNN1A
SCNN1B
SCNN1G


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


CLN11 disease
GRN
Idiopathic bronchiectasis
CFTR SCNN1A SCNN1B SCNN1G



CLN11 disease
Idiopathic bronchiectasis

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare respiratory disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the respiratory system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
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.