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

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


COMMON
GENES
CRYBB2
CRYGD
MIP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CRYAA
CRYAA
CRYAA
CRYBB2
GJA3
(0.88)
(0.78)
(0.77)
(0.65)
(0.52)
CRYBB2
CRYGD
MIP
MIP
MIP



Citations in the biomedical literature:


Nuclear cataract
CRYAA CRYBB1 CRYBB2 CRYBB3 CRYGD FYCO1
GJA3 MIP NHS WFS1
Cerulean cataract
MAF



Nuclear cataract
Cerulean cataract

Synonym(s):
(no synonyms)

Synonym(s):
- Blue-dot cataract

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- 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:
6 OMIM references -
1 MeSH reference: C537955

No signs/symptoms info available.