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Typical nemaline myopathy

5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Hereditary gingival fibromatosis

4 OMIM references -
1 associated gene
2 signs/symptoms

Typical nemaline myopathy

Hereditary gingival fibromatosis

ACTA1	(UniProt - OMIM)		SOS1	(UniProt - OMIM)
CFL2	(UniProt - OMIM)
KLHL41	(UniProt - OMIM)
NEB	(UniProt - OMIM)
TPM2	(UniProt - OMIM)


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

Citations in the biomedical literature:

Typical nemaline myopathy		Hereditary gingival fibromatosis
	Synonym(s): (no synonyms)		Synonym(s): - Autosomal dominant gingival fibromatosis - Autosomal dominant gingival hyperplasia - Hereditary gingival hyperplasia

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

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

	Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: normal Type of inheritance: autosomal dominant

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

Hereditary gingival fibromatosis
	Very frequent - Autosomal dominant inheritance - Thickened / hypertrophic / fibromatous gingivae
Typical nemaline myopathy
(no data available)