Cytoscape Web
Click node...

Hemimegalencephaly
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Phakomatosis pigmentokeratotica
1 associated gene
No signs/symptoms info
Hemimegalencephaly
Phakomatosis pigmentokeratotica

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

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PIK3CA
(0.95)
HRAS


Citations in the biomedical literature:


Hemimegalencephaly
AKT3 PIK3CA
Phakomatosis pigmentokeratotica
HRAS



Hemimegalencephaly
Phakomatosis pigmentokeratotica

Synonym(s):
- Unilateral megalencephaly
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- 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: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: unknown
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
1 MeSH reference: C537893
No signs/symptoms info available.