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

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


COMMON
GENES
CRYBB1
GJA3


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


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



Nuclear cataract
Pulverulent cataract

Synonym(s):
(no synonyms)

Synonym(s):
- Dusty 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:
7 OMIM references -
No MeSH references

No signs/symptoms info available.