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Hemimegalencephaly
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
1 OMIM reference -
2 associated genes
No signs/symptoms info
Hemimegalencephaly
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis

AKT3
(UniProt - OMIM)
 PKD1
(UniProt - OMIM)
PIK3CA
(UniProt - OMIM)
 TSC2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
AKT3
(0.55)
TSC2


Citations in the biomedical literature:


Hemimegalencephaly
AKT3 PIK3CA
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
PKD1 TSC2



Hemimegalencephaly
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis

Synonym(s):
- Unilateral megalencephaly
Synonym(s):
- Tuberous sclerosis/polycystic kidney disease contiguous gene syndrome
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.