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7 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
1 associated gene
2 signs/symptoms
Pilocytic astrocytoma
Hereditary gingival fibromatosis

BRAF SOS1
FGFR1
KIAA1549
KRAS
NTRK2
RAF1
SRGAP3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FGFR1
(0.52)
SOS1



Citations in the biomedical literature:


Pilocytic astrocytoma
BRAF FGFR1 KIAA1549 KRAS NTRK2 RAF1
SRGAP3
Hereditary gingival fibromatosis
SOS1



Pilocytic astrocytoma
Hereditary gingival fibromatosis

Synonym(s):
(no synonyms)

Synonym(s):
- Autosomal dominant gingival fibromatosis
- Autosomal dominant gingival hyperplasia
- Hereditary gingival hyperplasia

Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare genetic disease
- Rare odontologic disease

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

Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
4 OMIM references -
No MeSH references

Hereditary gingival fibromatosis

Very frequent
- Autosomal dominant inheritance
- Thickened / hypertrophic / fibromatous gingivae



Pilocytic astrocytoma

(no data available)