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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Alexander disease type II
Familial parathyroid adenoma

GFAP CDC73
MEN1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
GFAP
(0.88)
MEN1



Citations in the biomedical literature:


Alexander disease type II
GFAP
Familial parathyroid adenoma
CDC73 MEN1



Alexander disease type II
Familial parathyroid adenoma

Synonym(s):
- AxD type II

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare oncologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

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:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.