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7 OMIM references -
7 associated genes
No signs/symptoms info
COMMON GENES: 2
PROTEIN INTERACTIONS: 6
13 OMIM references -
10 associated genes
No signs/symptoms info
Pulverulent cataract
Nuclear cataract

CRYBB1 CRYAA
CRYGC CRYBB1
GJA3 CRYBB2
GJA8 CRYBB3
LIM2 CRYGD
MAF FYCO1
VIM GJA3
MIP
NHS
WFS1


COMMON
GENES
CRYBB1
GJA3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CRYGC
CRYGC
CRYGC
CRYGC
GJA3
GJA8
(0.89)
(0.88)
(0.65)
(0.63)
(0.52)
(0.52)
CRYAA
CRYBB2
MIP
CRYGD
MIP
MIP



Citations in the biomedical literature:


Pulverulent cataract
CRYBB1 CRYGC GJA3 GJA8 LIM2 MAF
VIM
Nuclear cataract
CRYAA CRYBB2 CRYBB3 CRYGD FYCO1
MIP NHS WFS1



Pulverulent cataract
Nuclear cataract

Synonym(s):
- Dusty cataract

Synonym(s):
(no synonyms)

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

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

No signs/symptoms info available.