ODCs

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

PROTEIN INTERACTIONS: 1

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

Autosomal recessive limb-girdle muscular dystrophy type 2J

Familial isolated restrictive cardiomyopathy


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

Citations in the biomedical literature:

Autosomal recessive limb-girdle muscular dystrophy type 2J		Familial isolated restrictive cardiomyopathy
	Synonym(s): - LGMD2J		Synonym(s): - Familial or idiopathic restrictive cardiomyopathy

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare cardiac disease - Rare genetic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the circulatory system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable Average age of death: any age Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 4 OMIM references - No MeSH references

No signs/symptoms info available.