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Pulverulent cataract
7 OMIM references -
7 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
1 associated gene
No signs/symptoms info
Pulverulent cataract
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency

CRYBB1
(UniProt - OMIM)
 ISG15
(UniProt - OMIM)
CRYGC
(UniProt - OMIM)
GJA3
(UniProt - OMIM)
GJA8
(UniProt - OMIM)
LIM2
(UniProt - OMIM)
MAF
(UniProt - OMIM)
VIM
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
VIM
(0.63)
ISG15


Citations in the biomedical literature:


Pulverulent cataract
CRYBB1 CRYGC GJA3 GJA8 LIM2 MAF
VIM
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
ISG15



Pulverulent cataract
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency

Synonym(s):
- Dusty cataract
Synonym(s):
- MSMD due to complete ISG15 deficiency
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal recessive
External references:
7 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.