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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Estrogen resistance syndrome
Hypoinsulinemic hypoglycemia and body hemihypertrophy

ESR1 AKT2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ESR1
(0.8)
AKT2



Citations in the biomedical literature:


Estrogen resistance syndrome
ESR1
Hypoinsulinemic hypoglycemia and body hemihypertrophy
AKT2



Estrogen resistance syndrome
Hypoinsulinemic hypoglycemia and body hemihypertrophy

Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.