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Familial multiple meningioma
1 OMIM reference -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital myopathy with excess of thin filaments
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial multiple meningioma
Congenital myopathy with excess of thin filaments

MN1
(UniProt - OMIM)
 ACTA1
(UniProt - OMIM)
PDGFB
(UniProt - OMIM)
SMARCB1
(UniProt - OMIM)
SMARCE1
(UniProt - OMIM)
SUFU
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SMARCB1
(0.63)
ACTA1


Citations in the biomedical literature:


Familial multiple meningioma
MN1 PDGFB SMARCB1 SMARCE1 SUFU
Congenital myopathy with excess of thin filaments
ACTA1



Familial multiple meningioma
Congenital myopathy with excess of thin filaments

Synonym(s):
(no synonyms)

Synonym(s):
- Actin myopathy
Classification (Orphanet):
- Rare neurologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.