ODCs

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6 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Childhood-onset nemaline myopathy

Progressive sensorineural hearing loss - hypertrophic cardiomyopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ACTA1	(0.52)	MYO6

Citations in the biomedical literature:

Childhood-onset nemaline myopathy		Progressive sensorineural hearing loss - hypertrophic cardiomyopathy
	Synonym(s): - Mild nemaline myopathy		Synonym(s): - Progressive neurosensory deafness - hypertrophic cardiomyopathy - Progressive neurosensory hearing loss - hypertrophic cardiomyopathy - Progressive sensorineural deafness - hypertrophic cardiomyopathy

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare cardiac disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare otorhinolaryngologic disease

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

	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: <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: 1 OMIM reference - No MeSH references

No signs/symptoms info available.