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Hemimegalencephaly
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Intermittent hydrarthrosis
2 associated genes
No signs/symptoms info
Hemimegalencephaly
Intermittent hydrarthrosis

AKT3
(UniProt - OMIM)
 MEFV
(UniProt - OMIM)
PIK3CA
(UniProt - OMIM)
 TNFRSF1A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PIK3CA
(0.63)
TNFRSF1A


Citations in the biomedical literature:


Hemimegalencephaly
AKT3 PIK3CA
Intermittent hydrarthrosis
MEFV TNFRSF1A



Hemimegalencephaly
Intermittent hydrarthrosis

Synonym(s):
- Unilateral megalencephaly
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)
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.