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Hereditary gingival fibromatosis

4 OMIM references -
1 associated gene
2 signs/symptoms

PROTEIN INTERACTIONS: 1

Severe congenital nemaline myopathy

4 associated genes
No signs/symptoms info

Hereditary gingival fibromatosis

Severe congenital nemaline myopathy

SOS1	(UniProt - OMIM)		ACTA1	(UniProt - OMIM)
			KLHL40	(UniProt - OMIM)
			KLHL41	(UniProt - OMIM)
			NEB	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SOS1	(0.79)	NEB

Citations in the biomedical literature:

Hereditary gingival fibromatosis		Severe congenital nemaline myopathy
	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 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: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: child / adolescent Type of inheritance: autosomal recessive

	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
Severe congenital nemaline myopathy
(no data available)