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1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
7 associated genes
No signs/symptoms info
Oculootodental syndrome
Pilocytic astrocytoma

FADD BRAF
FGF3 FGFR1
KIAA1549
KRAS
NTRK2
RAF1
SRGAP3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FGF3
(0.52)
FGFR1



Citations in the biomedical literature:


Oculootodental syndrome
FADD FGF3
Pilocytic astrocytoma
BRAF FGFR1 KIAA1549 KRAS NTRK2 RAF1
SRGAP3



Oculootodental syndrome
Pilocytic astrocytoma

Synonym(s):
- OOD

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare odontologic disease
Classification (Orphanet):
(no data available)

Classification (ICD10):
- Diseases of the digestive system -
Classification (ICD10):
(no data available)

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

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

No signs/symptoms info available.