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7 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Pilocytic astrocytoma
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion

BRAF CREBBP
FGFR1
KIAA1549
KRAS
NTRK2
RAF1
SRGAP3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FGFR1
(0.67)
CREBBP



Citations in the biomedical literature:


Pilocytic astrocytoma
BRAF FGFR1 KIAA1549 KRAS NTRK2 RAF1
SRGAP3
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
CREBBP



Pilocytic astrocytoma
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion

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

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

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

No signs/symptoms info available.