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Childhood-onset nemaline myopathy

6 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Hereditary gingival fibromatosis

4 OMIM references -
1 associated gene
2 signs/symptoms

Childhood-onset nemaline myopathy

Hereditary gingival fibromatosis

ACTA1	(UniProt - OMIM)		SOS1	(UniProt - OMIM)
KBTBD13	(UniProt - OMIM)
KLHL41	(UniProt - OMIM)
NEB	(UniProt - OMIM)
TPM2	(UniProt - OMIM)
TPM3	(UniProt - OMIM)


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

Citations in the biomedical literature:

Childhood-onset nemaline myopathy		Hereditary gingival fibromatosis
	Synonym(s): - Mild nemaline myopathy		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 / 1 000 000 Average age onset: childhood Average age of death: - 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
Childhood-onset nemaline myopathy
(no data available)