ODCs

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

PROTEIN INTERACTIONS: 1

6 associated genes
No signs/symptoms info

Progressive sensorineural hearing loss - hypertrophic cardiomyopathy

Childhood-onset nemaline myopathy


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

Citations in the biomedical literature:

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

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

	Classification (ICD10): (no data available)		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: childhood Average age of death: - 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.