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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Alpha-crystallinopathy
Alexander disease type I

CRYAB GFAP


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Alpha-crystallinopathy
CRYAB
Alexander disease type I
GFAP



Alpha-crystallinopathy
Alexander disease type I

Synonym(s):
- CRYAB-related myofobrillar myopathy

Synonym(s):
- AxD type I

Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.