ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Familial isolated restrictive cardiomyopathy

Amish nemaline myopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TNNI3	(0.52)	TNNT1

Citations in the biomedical literature:

Familial isolated restrictive cardiomyopathy		Amish nemaline myopathy
	Synonym(s): - Familial or idiopathic restrictive cardiomyopathy		Synonym(s): (no synonyms)

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

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

	Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable Average age of death: any age Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal recessive

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

No signs/symptoms info available.