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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
14q11.2 microduplication syndrome
Lipoprotein glomerulopathy

FOXG1 APOE


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FOXG1
(0.63)
APOE



Citations in the biomedical literature:


14q11.2 microduplication syndrome
FOXG1
Lipoprotein glomerulopathy
APOE



14q11.2 microduplication syndrome
Lipoprotein glomerulopathy

Synonym(s):
- Dup(14)(q11.2)
- Trisomy 14q11.2

Synonym(s):
- LPG

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare endocrine disease
- Rare genetic disease
- Rare renal disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.