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Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Hemimegalencephaly
2 associated genes
No signs/symptoms info
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Hemimegalencephaly

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

COMMON
GENES 		PIK3CA


Citations in the biomedical literature:


Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
PIK3CA
Hemimegalencephaly
AKT3



Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Hemimegalencephaly

Synonym(s):
(no synonyms)

Synonym(s):
- Unilateral megalencephaly
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.