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13 OMIM references -
10 associated genes
No signs/symptoms info
COMMON GENES: 3
PROTEIN INTERACTIONS: 4
7 OMIM references -
5 associated genes
No signs/symptoms info
Nuclear cataract
Total congenital cataract

CRYAA CRYBB2
CRYBB1 CRYGB
CRYBB2 EPHA2
CRYBB3 MIP
CRYGD NHS
FYCO1
GJA3
MIP
NHS
WFS1


COMMON
GENES
CRYBB2
MIP
NHS


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CRYAA
CRYAA
CRYBB2
GJA3
(0.88)
(0.77)
(0.65)
(0.52)
CRYBB2
MIP
MIP
MIP



Citations in the biomedical literature:


Nuclear cataract
CRYAA CRYBB1 CRYBB2 CRYBB3 CRYGD FYCO1
GJA3 MIP NHS WFS1
Total congenital cataract
CRYGB EPHA2



Nuclear cataract
Total congenital 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 -
1 MeSH reference: C535341

No signs/symptoms info available.