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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
5 associated genes
No signs/symptoms info
Rubinstein-Taybi syndrome due to CREBBP mutations
Familial multiple meningioma

CREBBP MN1
PDGFB
SMARCB1
SMARCE1
SUFU


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CREBBP
(0.83)
SMARCB1



Citations in the biomedical literature:


Rubinstein-Taybi syndrome due to CREBBP mutations
CREBBP
Familial multiple meningioma
MN1 PDGFB SMARCB1 SMARCE1 SUFU



Rubinstein-Taybi syndrome due to CREBBP mutations
Familial multiple meningioma

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare oncologic disease
- Rare renal disease
Classification (Orphanet):
- Rare neurologic disease
- Rare oncologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)

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

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

No signs/symptoms info available.