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Hereditary gingival fibromatosis

4 OMIM references -
1 associated gene
2 signs/symptoms

PROTEIN INTERACTIONS: 1

Hepatocellular carcinoma, childhood-onset

2 associated genes
No signs/symptoms info

Hereditary gingival fibromatosis

Hepatocellular carcinoma, childhood-onset

SOS1	(UniProt - OMIM)		CTNNB1	(UniProt - OMIM)
			MET	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SOS1	(0.72)	MET

Citations in the biomedical literature:

Hereditary gingival fibromatosis		Hepatocellular carcinoma, childhood-onset
	Synonym(s): - Autosomal dominant gingival fibromatosis - Autosomal dominant gingival hyperplasia - Hereditary gingival hyperplasia		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Diseases of the digestive system -		Classification (ICD10): - Neoplasms -

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

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

Hereditary gingival fibromatosis
	Very frequent - Autosomal dominant inheritance - Thickened / hypertrophic / fibromatous gingivae
Hepatocellular carcinoma, childhood-onset
(no data available)