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13 OMIM references -
10 associated genes
No signs/symptoms info
COMMON GENES: 3
PROTEIN INTERACTIONS: 8
4 OMIM references -
4 associated genes
No signs/symptoms info
Nuclear cataract
Coppock-like cataract

CRYAA CRYBB2
CRYBB1 CRYGC
CRYBB2 CRYGD
CRYBB3 GJA3
CRYGD
FYCO1
GJA3
MIP
NHS
WFS1


COMMON
GENES
CRYBB2
CRYGD
GJA3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CRYAA
CRYAA
CRYBB2
CRYAA
MIP
MIP
CRYGD
MIP
(0.89)
(0.88)
(0.88)
(0.78)
(0.65)
(0.65)
(0.63)
(0.52)
CRYGC
CRYBB2
CRYGC
CRYGD
CRYBB2
CRYGC
CRYGC
GJA3



Citations in the biomedical literature:


Nuclear cataract
CRYAA CRYBB1 CRYBB2 CRYBB3 CRYGD FYCO1
GJA3 MIP NHS WFS1
Coppock-like cataract
CRYGC



Nuclear cataract
Coppock-like cataract

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

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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:
4 OMIM references -
No MeSH references

No signs/symptoms info available.