ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

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

Tibial muscular dystrophy

Familial isolated restrictive cardiomyopathy


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

Citations in the biomedical literature:

Tibial muscular dystrophy		Familial isolated restrictive cardiomyopathy
	Synonym(s): - Distal myopathy, Udd type - Distal titinopathy - TMD - Udd myopathy		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: Class of prevalence: 1-9 / 100 000 Average age onset: adulthood Average age of death: normal Type of inheritance: autosomal dominant		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 - 1 MeSH reference: C536815		External references: 4 OMIM references - No MeSH references

No signs/symptoms info available.