ODCs

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4 OMIM references -
1 associated gene
2 signs/symptoms

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Hereditary gingival fibromatosis

Autosomal recessive centronuclear myopathy

SOS1	(UniProt - OMIM)		BIN1	(UniProt - OMIM)
			TTN	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SOS1	(0.7)	BIN1

Citations in the biomedical literature:

Hereditary gingival fibromatosis		Autosomal recessive centronuclear myopathy
	Synonym(s): - Autosomal dominant gingival fibromatosis - Autosomal dominant gingival hyperplasia - Hereditary gingival hyperplasia		Synonym(s): - AR-CNM

	Classification (Orphanet): - Rare genetic disease - Rare odontologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

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

	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: autosomal recessive

	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
Autosomal recessive centronuclear myopathy
(no data available)