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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Isolated focal cortical dysplasia type IIb
Isolated megalencephaly

TSC1 TBC1D7


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TSC1
(0.78)
TBC1D7



Citations in the biomedical literature:


Isolated focal cortical dysplasia type IIb
TSC1
Isolated megalencephaly
TBC1D7



Isolated focal cortical dysplasia type IIb
Isolated megalencephaly

Synonym(s):
- FCD type IIb

Synonym(s):
- Isolated macrencephaly

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare neurologic 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:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.