ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

5 associated genes
No signs/symptoms info

Congenital myopathy with excess of thin filaments

Typical nemaline myopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ACTA1	(0.56)	TPM2

Citations in the biomedical literature:

Congenital myopathy with excess of thin filaments		Typical nemaline myopathy
	Synonym(s): - Actin myopathy		Synonym(s): (no synonyms)

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant

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

No signs/symptoms info available.