ODCs

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2 OMIM references -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

4 associated genes
No signs/symptoms info

Cap myopathy

Severe congenital nemaline myopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TPM3 TPM2	(0.65) (0.56)	ACTA1 ACTA1

Citations in the biomedical literature:

Cap myopathy		Severe congenital nemaline myopathy
	Synonym(s): - Cap disease		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: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - 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: 2 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.