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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
Distal 17p13.3 microdeletion syndrome

TSC1 YWHAE


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TSC1
(0.76)
YWHAE



Citations in the biomedical literature:


Isolated focal cortical dysplasia type IIb
TSC1
Distal 17p13.3 microdeletion syndrome
YWHAE



Isolated focal cortical dysplasia type IIb
Distal 17p13.3 microdeletion syndrome

Synonym(s):
- FCD type IIb

Synonym(s):
- Distal del(17)(p13.3 )
- Distal monosomy 17p13.3

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic 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.