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Lennox-Gastaut syndrome
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Anaplastic ependymoma
2 associated genes
No signs/symptoms info
Lennox-Gastaut syndrome
Anaplastic ependymoma

CHD2
(UniProt - OMIM)
 C11ORF95
(UniProt - OMIM)
MAPK10
(UniProt - OMIM)
 RELA
(UniProt - OMIM)
SCN1A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MAPK10
(0.76)
RELA


Citations in the biomedical literature:


Lennox-Gastaut syndrome
CHD2 MAPK10 SCN1A
Anaplastic ependymoma
C11ORF95 RELA



Lennox-Gastaut syndrome
Anaplastic ependymoma

Synonym(s):
(no synonyms)

Synonym(s):
- High-grade ependymoma
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare neurologic disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
No OMIM references
1 MeSH reference: C535500
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.