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13 OMIM references -
10 associated genes
No signs/symptoms info
COMMON GENES: 2
PROTEIN INTERACTIONS: 8
4 OMIM references -
3 associated genes
No signs/symptoms info
Nuclear cataract
Cataract with Y-shaped suture opacities

CRYAA CRYBA1
CRYBB1 CRYBB2
CRYBB2 MIP
CRYBB3
CRYGD
FYCO1
GJA3
MIP
NHS
WFS1


COMMON
GENES
CRYBB2
MIP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CRYAA
CRYAA
CRYAA
CRYBB1
CRYBB2
CRYBB2
CRYBB3
GJA3
(0.88)
(0.77)
(0.76)
(0.73)
(0.65)
(0.63)
(0.63)
(0.52)
CRYBB2
MIP
CRYBA1
CRYBA1
MIP
CRYBA1
CRYBA1
MIP



Citations in the biomedical literature:


Nuclear cataract
CRYAA CRYBB1 CRYBB2 CRYBB3 CRYGD FYCO1
GJA3 MIP NHS WFS1
Cataract with Y-shaped suture opacities
CRYBA1



Nuclear cataract
Cataract with Y-shaped suture opacities

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.