ODCs

Click node...

4 associated genes
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 3

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

Intermediate nemaline myopathy

Cap myopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ACTA1 ACTA1 TPM3	(0.65) (0.56) (0.49)	TPM3 TPM2 TPM2

Citations in the biomedical literature:

Intermediate nemaline myopathy		Cap myopathy
	Synonym(s): (no synonyms)		Synonym(s): - Cap disease

	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: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 2 OMIM references - No MeSH references

No signs/symptoms info available.