Cytoscape Web
Click node...


7 OMIM references -
7 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Pulverulent cataract
Hyperinsulinism due to HNF1A deficiency

CRYBB1 HNF1A
CRYGC
GJA3
GJA8
LIM2
MAF
VIM


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Pulverulent cataract
CRYBB1 CRYGC GJA3 GJA8 LIM2 MAF
VIM
Hyperinsulinism due to HNF1A deficiency
HNF1A



Pulverulent cataract
Hyperinsulinism due to HNF1A deficiency

Synonym(s):
- Dusty cataract

Synonym(s):
- Hyperinsulinemic hypoglycemia due to HNF1A deficiency

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: <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:
No OMIM references
No MeSH references

No signs/symptoms info available.