ODCs

Click node...

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Adult-onset distal myopathy due to VCP mutation

Autosomal dominant Emery-Dreifuss muscular dystrophy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	VCP	(0.63)	LMNA

Citations in the biomedical literature:

Adult-onset distal myopathy due to VCP mutation		Autosomal dominant Emery-Dreifuss muscular dystrophy

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

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

No signs/symptoms info available.