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7 OMIM references -
7 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
11 OMIM references -
12 associated genes
No signs/symptoms info
Pulverulent cataract
MODY syndrome

CRYBB1 ABCC8
CRYGC BLK
GJA3 CEL
GJA8 GCK
LIM2 HNF1A
MAF HNF4A
VIM INS
KCNJ11
KLF11
NEUROD1
PAX4
PDX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
VIM
CRYBB1
(0.63)
(0.52)
HNF1A
ABCC8



Citations in the biomedical literature:


Pulverulent cataract
CRYBB1 CRYGC GJA3 GJA8 LIM2 MAF
VIM
MODY syndrome
ABCC8 BLK CEL GCK HNF1A HNF4A
INS KCNJ11 KLF11 NEUROD1 PAX4 PDX1



Pulverulent cataract
MODY syndrome

Synonym(s):
- Dusty cataract

Synonym(s):
- Maturity-onset diabetes of the young

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

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.