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13 OMIM references -
10 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
3 OMIM references -
4 associated genes
No signs/symptoms info
Nuclear cataract
Idiopathic bronchiectasis

CRYAA CFTR
CRYBB1 SCNN1A
CRYBB2 SCNN1B
CRYBB3 SCNN1G
CRYGD
FYCO1
GJA3
MIP
NHS
WFS1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
WFS1
NHS
(0.63)
(0.56)
CFTR
CFTR



Citations in the biomedical literature:


Nuclear cataract
CRYAA CRYBB1 CRYBB2 CRYBB3 CRYGD FYCO1
GJA3 MIP NHS WFS1
Idiopathic bronchiectasis
CFTR SCNN1A SCNN1B SCNN1G



Nuclear cataract
Idiopathic bronchiectasis

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

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

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

External references:
13 OMIM references -
No MeSH references
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.