Cytoscape Web
Click node...


13 OMIM references -
10 associated genes
No signs/symptoms info
COMMON GENES: 3
PROTEIN INTERACTIONS: 19
9 OMIM references -
9 associated genes
No signs/symptoms info
Nuclear cataract
Zonular cataract

CRYAA CRYAA
CRYBB1 CRYAB
CRYBB2 CRYBA1
CRYBB3 CRYBA4
CRYGD CRYGB
FYCO1 CRYGC
GJA3 CRYGD
MIP HSF4
NHS MIP
WFS1


COMMON
GENES
CRYAA
CRYGD
MIP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CRYAA
CRYAA
CRYBB2
CRYBB2
CRYBB2
CRYGD
CRYAA
CRYAA
CRYAA
CRYBB1
CRYBB2
MIP
MIP
CRYBB1
CRYBB2
CRYBB2
CRYBB3
CRYGD
GJA3
(0.99)
(0.89)
(0.89)
(0.88)
(0.88)
(0.79)
(0.78)
(0.77)
(0.76)
(0.73)
(0.65)
(0.65)
(0.65)
(0.63)
(0.63)
(0.63)
(0.63)
(0.63)
(0.52)
CRYAB
CRYGC
CRYAB
CRYAA
CRYGC
CRYAB
CRYGD
MIP
CRYBA1
CRYBA1
MIP
CRYAB
CRYGC
CRYBA4
CRYBA1
CRYBA4
CRYBA1
CRYGC
MIP



Citations in the biomedical literature:


Nuclear cataract
CRYAA CRYBB1 CRYBB2 CRYBB3 CRYGD FYCO1
GJA3 MIP NHS WFS1
Zonular cataract
CRYAB CRYBA1 CRYBA4 CRYGB CRYGC
HSF4



Nuclear cataract
Zonular cataract

Synonym(s):
(no synonyms)

Synonym(s):
- Lamellar 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:
9 OMIM references -
1 MeSH reference: C535342

No signs/symptoms info available.