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

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

COMMON
GENES 		PIK3CA


Citations in the biomedical literature:


CLOVE syndrome
PIK3CA
Hemimegalencephaly
AKT3



CLOVE syndrome
Hemimegalencephaly

Synonym(s):
- Congenital lipomatous overgrowth - vascular malformation - epidermal nevi
Synonym(s):
- Unilateral megalencephaly
Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.