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Hereditary gingival fibromatosis

4 OMIM references -
1 associated gene
2 signs/symptoms

PROTEIN INTERACTIONS: 1

Neurofibromatosis type 3

3 OMIM references -
3 associated genes
No signs/symptoms info

Hereditary gingival fibromatosis

Neurofibromatosis type 3

SOS1	(UniProt - OMIM)		LZTR1	(UniProt - OMIM)
			NF2	(UniProt - OMIM)
			SMARCB1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SOS1	(0.72)	NF2

Citations in the biomedical literature:

Hereditary gingival fibromatosis		Neurofibromatosis type 3
	Synonym(s): - Autosomal dominant gingival fibromatosis - Autosomal dominant gingival hyperplasia - Hereditary gingival hyperplasia		Synonym(s): - NF3 - Neurilemmomatosis - Schwannomatosis

	Classification (Orphanet): - Rare genetic disease - Rare odontologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease - Rare oncologic disease - Rare skin disease

	Classification (ICD10): - Diseases of the digestive system -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	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: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 4 OMIM references - No MeSH references		External references: 3 OMIM references - 1 MeSH reference: C536641

Hereditary gingival fibromatosis
	Very frequent - Autosomal dominant inheritance - Thickened / hypertrophic / fibromatous gingivae
Neurofibromatosis type 3
(no data available)