ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
1 sign/symptom

Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Autosomal recessive ataxia, Beauce type


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LMNA	(0.88)	SYNE1

Citations in the biomedical literature:

Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		Autosomal recessive ataxia, Beauce type
	Synonym(s): (no synonyms)		Synonym(s): - ARCA1 - Autosomal recessive cerebellar ataxia type 1 - SCAR8

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

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: no data available Type of inheritance: autosomal recessive

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

Autosomal recessive ataxia, Beauce type
	Very frequent - Ataxia / incoordination / trouble of the equilibrium
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
(no data available)