ODCs

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

PROTEIN INTERACTIONS: 1

2 OMIM references -
1 associated gene
No signs/symptoms info

Congenital myopathy with excess of thin filaments

Becker muscular dystrophy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ACTA1	(0.87)	DMD

Citations in the biomedical literature:

Congenital myopathy with excess of thin filaments		Becker muscular dystrophy
	Synonym(s): - Actin myopathy		Synonym(s): - BMD - Becker dystrophinopathy

	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: 1-9 / 100 000 Average age onset: childhood Average age of death: any age Type of inheritance: x-linked recessive

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: C537666

No signs/symptoms info available.