Cytoscape Web
Click node...

Hemimegalencephaly
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hemimegalencephaly
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

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

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PIK3CA
(0.85)
CBL


Citations in the biomedical literature:


Hemimegalencephaly
AKT3 PIK3CA
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
CBL



Hemimegalencephaly
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

Synonym(s):
- Unilateral megalencephaly
Synonym(s):
- CBL syndrome
- Noonan syndrome-like disorder with JMML
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
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:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.