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7 OMIM references -
7 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
4 associated genes
4 signs/symptoms
Pulverulent cataract
Microphthalmia - cataract

CRYBB1 CRYBA4
CRYGC SIX6
GJA3 TMEM114
GJA8 VSX2
LIM2
MAF
VIM


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CRYBB1
(0.63)
CRYBA4



Citations in the biomedical literature:


Pulverulent cataract
CRYBB1 CRYGC GJA3 GJA8 LIM2 MAF
VIM
Microphthalmia - cataract
CRYBA4 SIX6 TMEM114 VSX2



Pulverulent cataract
Microphthalmia - cataract

Synonym(s):
- Dusty cataract

Synonym(s):
- Congenital cataract - microphthalmia

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:
(no data available)

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

Microphthalmia - cataract

Frequent
- Anophthalmos / anophthalmia / microphthalmos / microphthalmia
- Autosomal dominant inheritance
- Coloboma of iris
- Retinoschisis / retinal / chorioretinal coloboma



Pulverulent cataract

(no data available)