ODCs

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

PROTEIN INTERACTIONS: 1

4 associated genes
No signs/symptoms info

Fibrosarcoma

Intermediate nemaline myopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ETV6	(0.55)	ACTA1

Citations in the biomedical literature:

Fibrosarcoma		Intermediate nemaline myopathy

	Classification (Orphanet): - Rare bone disease - Rare oncologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: D005354		External references: No OMIM references No MeSH references

No signs/symptoms info available.