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Posterior polar cataract
7 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant Charcot-Marie-Tooth disease type 2F
1 OMIM reference -
1 associated gene
No signs/symptoms info
Posterior polar cataract
Autosomal dominant Charcot-Marie-Tooth disease type 2F

CHMP4B
(UniProt - OMIM)
 HSPB1
(UniProt - OMIM)
CRYAB
(UniProt - OMIM)
EPHA2
(UniProt - OMIM)
GJA3
(UniProt - OMIM)
PITX3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CRYAB
(0.97)
HSPB1


Citations in the biomedical literature:


Posterior polar cataract
CHMP4B CRYAB EPHA2 GJA3 PITX3
Autosomal dominant Charcot-Marie-Tooth disease type 2F
HSPB1



Posterior polar cataract
Autosomal dominant Charcot-Marie-Tooth disease type 2F

Synonym(s):
- Posterior subcapsular cataract
Synonym(s):
- CMT2F
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
External references:
7 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.