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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
3 associated genes
No signs/symptoms info
Isolated focal cortical dysplasia type IIb
Neurofibromatosis type 3

TSC1 LZTR1
NF2
SMARCB1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TSC1
(0.52)
NF2



Citations in the biomedical literature:


Isolated focal cortical dysplasia type IIb
TSC1
Neurofibromatosis type 3
LZTR1 NF2 SMARCB1



Isolated focal cortical dysplasia type IIb
Neurofibromatosis type 3

Synonym(s):
- FCD type IIb

Synonym(s):
- NF3
- Neurilemmomatosis
- Schwannomatosis

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

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
3 OMIM references -
1 MeSH reference: C536641

No signs/symptoms info available.