ODCs

Click node...

4 OMIM references -
1 associated gene
2 signs/symptoms

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Hereditary gingival fibromatosis

Myeloid neoplasm associated with FGFR1 rearrangement


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

Citations in the biomedical literature:

Hereditary gingival fibromatosis		Myeloid neoplasm associated with FGFR1 rearrangement
	Synonym(s): - Autosomal dominant gingival fibromatosis - Autosomal dominant gingival hyperplasia - Hereditary gingival hyperplasia		Synonym(s): - 8p11 myeloproliferative syndrome - Stem cell leukemia/lymphoma

	Classification (Orphanet): - Rare genetic disease - Rare odontologic disease		Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease

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

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

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

Hereditary gingival fibromatosis
	Very frequent - Autosomal dominant inheritance - Thickened / hypertrophic / fibromatous gingivae
Myeloid neoplasm associated with FGFR1 rearrangement
(no data available)