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7 OMIM references -
7 associated genes
No signs/symptoms info
COMMON GENES: 4
PROTEIN INTERACTIONS: 4
3 OMIM references -
8 associated genes
9 signs/symptoms
Pulverulent cataract
Cataract-microcornea syndrome

CRYBB1 CRYAA
CRYGC CRYBA4
GJA3 CRYBB1
GJA8 CRYBB2
LIM2 CRYGC
MAF CRYGD
VIM GJA8
MAF


COMMON
GENES
CRYBB1
CRYGC
GJA8
MAF


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CRYGC
CRYGC
CRYBB1
CRYGC
(0.89)
(0.88)
(0.63)
(0.63)
CRYAA
CRYBB2
CRYBA4
CRYGD



Citations in the biomedical literature:


Pulverulent cataract
CRYBB1 CRYGC GJA3 GJA8 LIM2 MAF
VIM
Cataract-microcornea syndrome
CRYAA CRYBA4 CRYBB2 CRYGD



Pulverulent cataract
Cataract-microcornea syndrome

Synonym(s):
- Dusty cataract

Synonym(s):
(no synonyms)

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:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

External references:
7 OMIM references -
No MeSH references
External references:
3 OMIM references -
1 MeSH reference: C538287

Cataract-microcornea syndrome

Very frequent
- Autosomal dominant inheritance
- Autosomal recessive inheritance
- Cataract / lens opacification
- Microcornea

Frequent
- Myopia

Occasional
- Coloboma of iris
- Corneal clouding / opacity / vascularisation
- Corneal dystrophy
- Nystagmus


Pulverulent cataract

(no data available)