ODCs

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

PROTEIN INTERACTIONS: 1

4 associated genes
No signs/symptoms info

Miyoshi myopathy

Intermediate nemaline myopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DYSF	(0.65)	NEB

Citations in the biomedical literature:

Miyoshi myopathy		Intermediate nemaline myopathy

	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 / 1 000 000 Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant

	External references: 3 OMIM references - 1 MeSH reference: C537480		External references: No OMIM references No MeSH references

No signs/symptoms info available.