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7 OMIM references -
7 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Pulverulent cataract
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form

CRYBB1 CTNNA3
CRYGC DSC2
GJA3 DSG2
GJA8 DSP
LIM2 JUP
MAF LMNA
VIM PKP2
RYR2
TGFB3
TMEM43
TTN


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
VIM
VIM
(0.78)
(0.63)
DSP
PKP2



Citations in the biomedical literature:


Pulverulent cataract
CRYBB1 CRYGC GJA3 GJA8 LIM2 MAF
VIM
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
CTNNA3 DSC2 DSG2 DSP JUP LMNA
PKP2 RYR2 TGFB3 TMEM43 TTN



Pulverulent cataract
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form

Synonym(s):
- Dusty cataract

Synonym(s):
- Familial isolated arrhythmogenic ventricular cardiomyopathy, biventricular form

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the circulatory system -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

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

No signs/symptoms info available.