ODCs

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

PROTEIN INTERACTIONS: 1

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

Miyoshi myopathy

Early-onset myopathy with fatal cardiomyopathy

ANO5	(UniProt - OMIM)		TTN	(UniProt - OMIM)
DYSF	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DYSF	(0.63)	TTN

Citations in the biomedical literature:

Miyoshi myopathy		Early-onset myopathy with fatal cardiomyopathy

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare cardiac disease - 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: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.