Cytoscape Web
Click node...

Hemimegalencephaly
2 associated genes
No signs/symptoms info
COMMON GENES: 1
CLOVE syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hemimegalencephaly
CLOVE syndrome

AKT3
(UniProt - OMIM)
 PIK3CA
(UniProt - OMIM)
PIK3CA
(UniProt - OMIM)

COMMON
GENES 		PIK3CA


Citations in the biomedical literature:


Hemimegalencephaly
AKT3 PIK3CA
CLOVE syndrome



Hemimegalencephaly
CLOVE syndrome

Synonym(s):
- Unilateral megalencephaly
Synonym(s):
- Congenital lipomatous overgrowth - vascular malformation - epidermal nevi
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
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: sporadic
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.