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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
7 OMIM references -
5 associated genes
No signs/symptoms info
Alexander disease type II
Posterior polar cataract

GFAP CHMP4B
CRYAB
EPHA2
GJA3
PITX3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
GFAP
(0.56)
CRYAB



Citations in the biomedical literature:


Alexander disease type II
GFAP
Posterior polar cataract
CHMP4B CRYAB EPHA2 GJA3 PITX3



Alexander disease type II
Posterior polar cataract

Synonym(s):
- AxD type II

Synonym(s):
- Posterior subcapsular cataract

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

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: adult
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

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

No signs/symptoms info available.