ODCs

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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

Lethal congenital contracture syndrome type 2


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SOS1	(0.55)	ERBB3

Citations in the biomedical literature:

Hereditary gingival fibromatosis		Lethal congenital contracture syndrome type 2
	Synonym(s): - Autosomal dominant gingival fibromatosis - Autosomal dominant gingival hyperplasia - Hereditary gingival hyperplasia		Synonym(s): - LCCS2 - Multiple contracture syndrome, Israeli-Bedouin type

	Classification (Orphanet): - Rare genetic disease - Rare odontologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic 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: (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
Lethal congenital contracture syndrome type 2
(no data available)